In 2019 J ORG CHEM published article about FRIEDEL-CRAFTS ALKENYLATION; STEREOSELECTIVE-SYNTHESIS; ARYLBORONIC ACIDS; TERMINAL ALKYNES; VINYL-ACETATE; TRISUBSTITUTED ALKENES; ORGANOZINC REAGENTS; GRIGNARD-REAGENTS; INTERNAL ALKYNES; CIS-INSERTION in [Barber, E. Ryan; Hynds, Hannah M.; Stephens, Claudia P.; Lemons, Holli E.; Fredrickson, Emily T.; Wilger, Dale J.] Samford Univ, Dept Chem & Biochem, Birmingham, AL 35229 USA in 2019, Cited 96. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. Quality Control of 1-Chloro-2-methylbenzene
An operationally simple nickel-catalyzed hydroarylation reaction for alkynes is described. This three component coupling reaction utilizes commercially available alkynes and aryl bromides, along with water and Zn. An air-stable and easily synthesized Ni(II) precatalyst is the only entity used in the reaction that is not commercially available. This reductive cross-coupling reaction displays a fairly unusual anti selectivity when aryl bromides with ortho substituents are used. In addition to optimization data and a preliminary substrate scope, complementary experiments including deuterium labeling studies are used to provide a tentative catalytic mechanism. We believe this report should inspire and inform other Ni-catalyzed carbofunctionalization reactions.
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Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
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