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【结 构 式】

【分子编号】33852

【品名】2-bromo-N-(4-chlorophenyl)-N-(2,2,2-trifluoroethyl)acetamide

【CA登记号】

【 分 子 式 】C10H8BrClF3NO

【 分 子 量 】330.5315696

【元素组成】C 36.34% H 2.44% Br 24.17% Cl 10.73% F 17.24% N 4.24% O 4.84%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(XVI)

N-bromoacetyl compound (IV) can also be obtained by bromoacetylation of (XV) with bromoacetyl bromide (B) in refluxing benzene affording 4-chloro-N-bromoacetyl-N-(2,2,2-trifluoroethyl)aniline (XVI), followed by a Friedel-Crafts reaction with benzoyl chloride by means of AlCl3.

1 Topliss, J.G.; 2-Polyfluoroweralkyl benzophenones. US 3641147 .
2 Topliss, J.G.; 1-Polyhalogenoalkyl-2-oxo-1,3-dihydro-2H-14-benzodiazepines. US 3429874 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(D) 10463 Benzoyl chloride 98-88-4 C7H5ClO 详情 详情
(B) 14005 2-Bromoacetyl bromide; Bromoacetyl bromide 598-21-0 C2H2Br2O 详情 详情
(IV) 33849 N-(2-benzoyl-4-chlorophenyl)-2-bromo-N-(2,2,2-trifluoroethyl)acetamide C17H12BrClF3NO2 详情 详情
(XV) 33475 N-(4-chlorophenyl)-N-(2,2,2-trifluoroethyl)amine; 4-chloro-N-(2,2,2-trifluoroethyl)aniline C8H7ClF3N 详情 详情
(XVI) 33852 2-bromo-N-(4-chlorophenyl)-N-(2,2,2-trifluoroethyl)acetamide C10H8BrClF3NO 详情 详情
Extended Information