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HRID 382504作成日:2026年10月27日

Hydrochloric Acid → (2-Chloro-6-fluorophenyl)-P-tolyl-amine

https://huagongshe.com/reaction/382504

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物p-ToluidineHCID 7813—
反応物Binap, (A+-)-HCID 634876—
反応物2-Bromo-1-chloro-3-fluorobenzeneHCID 21938660—
反応物Sodium t-butoxideHCID 23676156—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物(2-Chloro-6-fluorophenyl)-P-tolyl-amineHCID 21100364—

反応手順

A mixture of 146.1 g (1.36 mol) of p-toluidine, 12.6 g (0.02 mol) of (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 261.9 g (2.73 mol) of sodium t-butoxide, 314.1 g (1.50 mol) of 2-bromo-3-fluoro-chlorobenzene and 6.3 g (0.0069 mol) of tris(dibenzylideneacetone)dipalladium(0) in 3000 ml of toluene is heated to 110° over 30 minutes and stirred an additional 4 hours at this temperature. The mixture is cooled to room temperature and a solution of 680 ml 37% hydrochloric acid and 680 ml of water is added over 15 minutes. The mixture is stirred for 20 minutes and filtered through a pad of Celite. The layers are separated and the organic phase is washed twice with 680 ml of water and once with a solution of 225 g of sodium chloride in 680 ml of water. The solvents are evaporated under reduced pressure to give N-(2′-chloro-6′-fluorophenyl)-4-methylaniline as an oil, b.p. 129-131°/0.5 mm Hg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06310099B1
出典データセットuspto-grants-2001_10
ORD IDord-7217a856ac394162acba3a03aaf6d4f1
出典メモuspto-grants-2001_10