Réaction #59156

Équation de réaction

trans-3-(4-bromobenzoyl)cyclohexane-l-carboxylic acid

2,2-dimethoxypropane

→

3-(4-bromo-benzoyl)-cyclohexanecarboxylic acid methyl ester

Rendement 95.7%

Solvants

methanol

dioxane

Conditions de réaction

Traitement

1. 1
   AutreThe solvent was removed by rotary evaporation

Mode opératoire

To a solution of trans-3-(4-bromobenzoyl)cyclohexane-l-carboxylic acid (500 mg, 1.61 mmol, obtained from Rieke Metals Inc., Lincoln, Nebr., USA) and 2,2-dimethoxypropane (669 mg, 6.43 mmol) in methanol (20 mL), 5 drops of 4 M HCl in dioxane was added, and this reaction mixture was heated at 50° C. overnight. The solvent was removed by rotary evaporation to give the product 3-(4-bromo-benzoyl)-cyclohexanecarboxylic acid methyl ester as a brown oil (500 mg, yield 95.7%). 1H NMR (300 MHz, DMSO) δ 7.80 (d, 2H), 7.60 (d, 2H), 3.70 (s, 3H), 3.25 (m, 1 H), 2.50 (m, 1H), 2.20-1.90 (m, 4H), 1.70-1.50 (m, 4H); LC-MS ret. time 3.30 min, m/z 324.9 (MH+).

Source