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HRID 78330作成日:2026年10月25日

4-Chloro-3-(trifluoromethyl)aniline → Ethyl 4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)benzoate

https://huagongshe.com/reaction/78330

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
反応物Ethyl 4-isocyanatobenzoateHCID 589805—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)benzoateHCID 221221897%

反応手順

To a solution of ethyl 4-isocyanatobenzoate (3.14 g, 16.4 mmol) in CH2Cl2 (30 mL) was added 4-chloro-3-(trifluoromethyl)aniline (3.21 g, 16.4 mmol), and the solution was stirred at room temp. overnight. The resulting slurry was diluted with CH2Cl2 (50 mL) and filtered to afford N-(4-chloro-3-(trifluoromethyl)phenyl)-N′-(4-ethoxycarbonylphenyl)urea as a white solid (5.93 g, 97%): TLC (40% EtOAc/60% hexane) Rf 0.44.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841330B2
出典データセットuspto-grants-2014_09
ORD IDord-99b39eae20d145379a672358c08bdaf8
出典メモuspto-grants-2014_09