Tag: M.W=100-200

Related Products of 108-70-3,Some common heterocyclic compound, 108-70-3, name is 1,3,5-Trichlorobenzene, molecular formula is C6H3Cl3, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

EXAMPLE 1; [0099] 3,5-Dichlorophenyl-isopropylsulfide (2); EMI20.0[0100] Method A; [0101] To a solution of 4N sodium hydroxide (0.8 ml) was added isopropylmercaptan (0.33 ml). The mixture was stirred for 10 minutes at room temperature. 1,3,5-Trichlorobenzene(1) (1.8 g, 10 mmol) and tetra n-butylammoniumbromide (322 mg, 1 mmol) were added thereto. The reaction mixture was refluxed under vigorous stirring at 140[deg.] C. for 5.5 hours. The reaction mixture was poured into ice-water, extracted with ethylacetate, washed with water, dried over sodium sulphate, filtrated and concentrated under reduced pressure. The obtained residue was chromatographed twice on silica gel (SiO2 18 g, elution: n-hexane) to yield the objective (2) (566 mg). Yield 85%. [0102] IR(film) 1555, 1400, 1375, 1360, 1155 cm<-1>. [0103] <1>H-NMR (CDCl3, 200 MHz) [delta]: 1.32 (6H, d, J=6.4 Hz), 3.42 (1H, sept, J=6.4 Hz), 7.15-7.25 (3H, m).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 1,3,5-Trichlorobenzene, its application will become more common.

Reference:
Patent; Aoki, Tsutomu; Konoike, Toshiro; US2003/195363; (2003); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 104-11-0, name is 1-(4-Chlorophenyl)-N-methylmethanamine, This compound has unique chemical properties. The synthetic route is as follows., Application In Synthesis of 1-(4-Chlorophenyl)-N-methylmethanamine

General procedure: A solution of 0.17g (1.40mmol) of N-benzylmethylamine, 0.20g (1.40mmol) of K2CO3 and 0.40g of (R,S)-3(4-bromobutyl)-5-phenyloxazolidin-2-one 23 in ACN was allowed to stirring under reflux for 6-12h and monitored by TLC until the reaction was completed. The hot solution was filtered and concentrated in vacuo to afford 0.29g (85.0mmol) of a chromatography pure yellow oil 2a.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 104-11-0.

Reference:
Article; Zampieri, Daniele; Vio, Luciano; Fermeglia, Maurizio; Pricl, Sabrina; Wuensch, Bernhard; Schepmann, Dirk; Romano, Maurizio; Mamolo, Maria Grazia; Laurini, Erik; European Journal of Medicinal Chemistry; vol. 121; (2016); p. 712 – 726;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Related Products of 6775-78-6, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 6775-78-6, name is 6-Chloroimidazo[1,2-b]pyridazine belongs to chlorides-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

3-bromo-6-chloroimidazo[l,2-b]pyridazine (11-1) was synthesized as shown in scheme 11, wherein N-bromosuccinamide (19.2 g, 108 mmol) was added to a solution of chloro-imidazo[l,2- b]pyridazine (10-1) (15 g, 98 mmol) in DMF cooled to 00C. The resulting solution was stirred at 00C for 1 hour and the reaction mixture was then poured into 1.4L of stirring water at room temperature. The resulting yellow heterogeneous solution was then stirred at room temperature for one hour and the solids were then filtered and washed with hexanes. The solid was dried under vacuum over-night to yield 3- bromo-6-chloroimidazo[l,2-b]pyridazine (11-1) as a yellow solid.

The synthetic route of 6-Chloroimidazo[1,2-b]pyridazine has been constantly updated, and we look forward to future research findings.

Reference:
Patent; IRM LLC; WO2009/140128; (2009); A2;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Application of 53145-38-3, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 53145-38-3, name is 2-Chloro-6-fluoroanisole, This compound has unique chemical properties. The synthetic route is as follows.

Under N2 atmosphere, an oven-dried 4 mL vial was charged with l-chloro-3- fluoro-2-methoxybenzene (48.2 mg, 38.9 mu, 0.300 mmol, 1.00 equiv), palladium complex 1 (11.4 mg, 15.0 muetaiotaomicron, 5.00 mol%), Ag(bipy)2C104 (16.0 mg, 30.0 muetaiotaomicron, 10.0 mol%), and NFBS (0.189 g, 0.600 mmol, 2.00 equiv). Acetonitrile (0.75 mL, c = 0.40 M) was added and the reaction mixture was stirred in a sealed vial at 23 C for 24 h. Subsequently, triethylamine (30.5 mg, 42.0 mu, 0.300 mmol, 1.00 equiv) was added and the reaction mixture was concentrated in vacuo. The residue was purified by chromatography on silica gel, eluting with hexanes/EtOAc (19: 1 to 4: 1 (v/v) with 1% triethylamine), to afford 106.7 mg of a mixture of the title compound and its two constitutional isomers (78% yield). Purification for characterization was accomplished by preparative TLC. [00221] Data for 2k: colorless solid; R/ = 0.59 (hexanes/EtOAc 7:3 (v/v)). NMR Spectroscopy: 1H NMR (600 MHz, CDC13, 23 C, delta): 7.93-7.97 (m, 4H), 7.70-7.74 (m, 2H), 7.57-7.61 (m, 4H), 6.83 (t, J = 2.1 Hz, 1H), 6.72 (dd, J = 10.9, 2.6 Hz, 1H), 4.04 (d, J = 2.3 Hz, 3H). 13C NMR (125 MHz, CDC13, 23 C, delta): 155.1 (d, J = 251.3 Hz), 146.4 (d, J = 12.5 Hz), 139.1, 134.5, 129.4, 129.1 (d, J = 3.8 Hz), 128.8 (d, J = 1.1 Hz), 128.7, 128.4 (d, J = 5.5 Hz), 119.4 (d, J =20 Hz), 61.7 (d, J = 6.3 Hz). 19F NMR (375 MHz, CDC13, 23 C, delta): -129.0 (d, J = 9.8 Hz). Mass Spectrometry: HRMS (ESI-TOF) (m/z): calcd for [M + NH4]+, 473.0402, found, 473.0415.

The chemical industry reduces the impact on the environment during synthesis 2-Chloro-6-fluoroanisole. I believe this compound will play a more active role in future production and life.

Reference:
Patent; PRESIDENT AND FELLOWS OF HARVARD COLLEGE; NGAI, Ming-Yu; BOURSALIAN, Gregory, Bagrad; MCNEILL, Eric, Andrew; RITTER, Tobias; WO2015/31725; (2015); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Adding a certain compound to certain chemical reactions, such as: 694-80-4, name is 1-Bromo-2-chlorobenzene, belongs to chlorides-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 694-80-4, Quality Control of 1-Bromo-2-chlorobenzene

General procedure: A 10 mL Schlenk tube equipped with a magnetic stirring bar was charged with 2-arylimidazo[1,2-a]pyridine 1 (0.2 mmol, 1.0 equiv), o-dihaloarene2 (0.3 mmol, 1.5 equiv), and K2CO3 (82.9 mg, 0.6 mmol, 3.0 equiv). To this mixture were added Pd(OAc)2 (0.02 mmol, 4.5 mg)and Xphos (0.04 mmol, 19.1 mg), followed by DMF (2.0 mL) via a syringe at r.t. The tube was sealed and kept in a preheated oil bath at 160 C for 24 h. The mixture was cooled to r.t., quenched with H2O (5mL), and diluted with CH2Cl2 (10 mL). The layers were separated and the aqueous layer was extracted with CH2Cl2 (3 × 5 mL). The combined organic extracts were dried (Na2SO4), filtered, and concentrated in vacuo. The crude product was then purified by flash chromatography on silica gel (H), eluting with 5-20% EtOAc-petroleum ether.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.

Reference:
Article; Wang, Hanyang; Chen, Chunxia; Huang, Zhangjie; Yao, Liping; Li, Bin; Peng, Jinsong; Synthesis; vol. 47; 16; (2015); p. 2457 – 2466;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Some common heterocyclic compound, 13078-79-0, name is 2-(3-Chlorophenyl)ethanamine, molecular formula is C8H10ClN, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. Safety of 2-(3-Chlorophenyl)ethanamine

General procedure: 4.2.1. General procedure for the preparation of final target compounds The intermediate free acid (1 equiv) was dissolved in CH2Cl2(7 mL) followed by the addition of triethylamine (2.2 equiv). Thereaction was cooled to 0 C and stirred for 30 min. Then phenethy-lamine (1.1 equiv) and 4-dimethylaminopyridine (DMAP) (cat.,0.1 equiv) were added to the solution followed by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC-HCl)(1.1 equiv) in ve portions over 20 min. The solution stirred at0 C for 1 h then overnight at rt. The resulting solution was dis-solved in an additional CH2Cl2 (25 mL), and washed with sat. NH4-Cl (10 mL). The aqueous layer was extracted with CH2Cl2(3 10 mL), organic layers combined, and sequentially washedwith 20 mL of each of the following: sat. NaHCO3,H2O, brine. Theorganic layer was dried over Na2SO4 and concentrated to give aresidue which was further puried with Celite (100% ethyl acet-ate). Then, the sample was dissolved in EtOAc, solution was heated,and cooled to 0 C. The solution was ltered to yield desiredproduct.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 13078-79-0, its application will become more common.

Reference:
Article; Gromek, Samantha M.; deMayo, James A.; Maxwell, Andrew T.; West, Ashley M.; Pavlik, Christopher M.; Zhao, Ziyan; Li, Jin; Wiemer, Andrew J.; Zweifach, Adam; Balunas, Marcy J.; Bioorganic and Medicinal Chemistry; vol. 24; 21; (2016); p. 5183 – 5196;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Adding a certain compound to certain chemical reactions, such as: 6940-78-9, name is 1-Bromo-4-chlorobutane, belongs to chlorides-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 6940-78-9, Computed Properties of C4H8BrCl

General procedure: To a solution of 4-nitrophenol (10 mmol, 1.0 eq) in 25 mL acetonitrile was added K2CO3 (10 mmol, 1 eq) at room temperature and stirred for 30 min, afterwards, different haloalkanes (15 mmol, 1.5 eq) were added dropwise. 1-Bromo-2-chloroethane (for 24a, n = 2); 1-bromo-3-chloropropane (for 24b, n = 3); 1-bromo-4-chlorobutane (for 24c, n = 4). The mixtures were stirred at 80 C for 12-24 h. The reactions were monitoring with TLC (petroleum ether: EtOAc = 4:1). Upon completion, water was added, the aqueous layer was extracted with EtOAc (25 mL × 3) and the combined organic layers were washed with brine. Evaporated the solvent to give the crude products 24a-c.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.

Reference:
Article; Zhai, Zheng; Li, Ridong; Bai, Xinyu; Ning, Xianling; Lin, Zhiqiang; Zhao, Xuyang; Jin, Yan; Yin, Yuxin; Bioorganic and Medicinal Chemistry; vol. 27; 18; (2019); p. 4124 – 4142;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Adding a certain compound to certain chemical reactions, such as: 367-22-6, name is 4-Chloro-3-fluoroaniline, belongs to chlorides-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 367-22-6, SDS of cas: 367-22-6

General procedure: To a stirred solution of anilines (3.29 mmol) in dichloromethane (6 mL) was added triethylamine (9.89 mmol) at room temperature and stirred at room temperature for 10 min and added aryl chloro formate (4.93 mmol) at 0 C and stirred at room temperature for 2 h. The reaction mixture was concentrated under reduced pressure and the crude material washed with 10 % diethyl ether in pentane to afford the pure compounds. Without further purification used for next step. Yields of the products varied between 65 to 85 %.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 4-Chloro-3-fluoroaniline, and friends who are interested can also refer to it.

Reference:
Article; Bhasker, G Vijaya; Satyanarayana; Latha; Laxminarayana; Chary, M Thirumala; Asian Journal of Chemistry; vol. 30; 4; (2018); p. 771 – 774;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Electric Literature of 694-80-4, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 694-80-4, name is 1-Bromo-2-chlorobenzene belongs to chlorides-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

General procedure: A mixture of the aryl halide(1 mmol), phenylboronic acid (0.1463 g, 1.2 mmol) or Ph4BNa (0.0855 g, 0.25 mmol),K2CO3 (0.2764 g, 2 mmol), ortho-palladated complex (0.0006 g, 0.1 mmol%) was addedto ethanol (2 ml) in round-bottom flask equipped with condenser and placed into theMilestone microwave oven. Initially the microwave irradiation was set at 600 W and thetemperature was raised to the desired temperature of 60C and the reaction mixture washeld at this temperature until the reaction was completed. The direct control of reactionmixture temperature was carried out using the IR sensors and software that enables on-linetemperature-pressure control by regulation of microwave power output. The mixture wasstirred continuously during the reaction and monitored by both TLC and GC. After thereaction was completed, the mixture was cooled to room temperature and was diluted withether (2 × 10 ml) and water (10 ml). The organic phase was dried overMgSO4, filtered andconcentrated under reduced pressure using a rotary evaporator. The residue was purified bysilica gel column chromatography (n-hexane:EtOAc, 9:1). The products were characterizedby comparing their mp., IR, 1H, 13C NMR spectra with those reported in the literature.Also Suzuki cross coupling reaction was carried out successfully in larger scale(30 mmol of aryl halide) using this ortho-palladated complex (0.018 g).

The synthetic route of 1-Bromo-2-chlorobenzene has been constantly updated, and we look forward to future research findings.

Reference:
Article; Hajipour, Abdol Reza; Rafiee, Fatemeh; Organic Preparations and Procedures International; vol. 45; 6; (2013); p. 465 – 472;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 102-49-8, name is 3,4-Dichlorobenzylamine, This compound has unique chemical properties. The synthetic route is as follows., Recommanded Product: 3,4-Dichlorobenzylamine

General procedure: The acid (9a?h) (1 mmol) and amine (1 mmol) were dissolvedin dimethylformamide (5v) under argon atmosphereand N-ethyl diisopropylamine (3 mmol) was added dropwise to it at 0 °C and HATU (1.3 mmol) was added lot wiseduring a period of 15 min. The reaction medium was slowlyallowed to reach room temperature and stirred for 4 h atroom temperature. The reaction progress was monitored byTLC. After completion of the reaction, the reaction mixturewas poured to ice cold water and stirred at room temperaturefor 30 min and the precipitated solid was filtered,washed with water and dried under vacuum. This crudeproduct was further purified by column chromatographyusing 2?5percent of methanol in chloroform to get the requiredamide.#10;

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 102-49-8.

Reference:
Article; Ajeesh Kumar; Bodke, Yadav D.; Lakra, Peter Serjious; Sambasivam, Ganesh; Bhat, Kishore G.; Medicinal Chemistry Research; vol. 26; 4; (2017); p. 714 – 744;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics