Reaction #1929077

Reaction equation

(4′-chloro-4-methylbiphenyl-3-yl)acetic acid

thionyl chloride

→

(4′-chloro-4-methylbiphenyl-3-yl)acetyl chloride

Yield 100.9%

Conditions

Workup

1. 1
   Concentrationconcentrated under reduced pressure
2. 2
   OtherDrying under fine vacuum

Procedure

5.00 g (19.18 mmol) of (4′-chloro-4-methylbiphenyl-3-yl)acetic acid (EP 2029531 A1 and US 2009/298828 A1) were dissolved in 36.51 g (306.84 mmol) of thionyl chloride. The reaction mixture was stirred at 80° C. for four hours and then concentrated under reduced pressure. Drying under fine vacuum gave 5.4 g (100% of theory) of (4′-chloro-4-methylbiphenyl-3-yl)acetyl chloride as a brownish oil. At room temperature, 5.00 g (19.09 mmol) of methyl cis-1-amino-4-(trifluoromethyl)cyclohexanecarboxylate hydrochloride (EP 1220841 A2 and WO 2001/23354 A3), 4.83 g (47.73 mmol) of triethylamine and 117 mg (0.955 mmol) of N,N-dimethylaminopyridine were dissolved in 40 ml of dichloromethane. A solution of 5.33 g (19.09 mmol) of (4′-chloro-4-methylbiphenyl-3-yl)acetyl chloride in 40 ml of dichloromethane was then added dropwise to the mixture. The resulting reaction mixture was stirred at room temperature overnight. For work-up, the mixture was diluted with dichloromethane and the organic phase was washed with aqueous 5% strength citric acid. After drying over sodium sulfate, the mixture was concentrated by evaporation and the residue was purified by chromatography on silica gel (mobile phase: hexane/ethyl acetate gradient). Concentration and drying gave 6.36 g (71% of theory) of the title compound.

Source