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HRID 393510作成日:2026年10月25日

N,N-Dimethylaniline → 2-(4-Nitrophenyl)-ethyl [4-(phenylamino)phenyl]-carbamate

https://huagongshe.com/reaction/393510

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylanilineHCID 949—
反応物N-Phenyl-p-phenylenediamineHCID 7564—
反応物TriphosgeneHCID 94429—
反応物1-(4-Nitrophenyl)ethan-1-olHCID 592376—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Nitrophenyl)-ethyl [4-(phenylamino)phenyl]-carbamateHCID 1214685922%

反応条件

温度20 °C

反応手順

1.18 g (3.9 mmol) of triphosgene is dissolved in 15 ml of dichloromethane in a 250 ml flask, under argon,. Using a motorized syringe, a solution of 2 g (12 mmol) of 4-nitrophenylethanol and 1.7 ml (13 mmol) of N,N-dimethylaniline in 40 ml of dichloromethane is added over 1 hour. The reaction mixture is agitated for a few minutes at 20° C. before adding in one go a solution of 2.2 g (12 mmol) of 4-aminodiphenylamine and 1.7 ml (13 mmol) of N,N-dimethylaniline in 40 ml of dichloromethane. After agitation for one hour at 20° C., the contents of the flask are poured into 100 ml of water. The mixture is diluted with 100 ml of dichloromethane and agitated. The organic phase is decanted, dried over magnesium sulphate, filtered and evaporated under vacuum. The solid obtained is taken up in ethyl ether, triturated and filtered. After drying, a greenish powder is obtained with a yield of 22%. Melting point: 146.4-148° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06809090B2
出典データセットuspto-grants-2004_10
ORD IDord-71b404e4407741cc956e2159a2b2afad
出典メモuspto-grants-2004_10