戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 589830作成日:2026年10月26日

Diisopropylethylamine → 4-Nitrophenyl 4,4,4-trifluorobutylcarbamate

https://huagongshe.com/reaction/589830

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-Nitrophenyl chloroformateHCID 82129—
反応物4,4,4-TrifluorobutylamineHCID 136645—
反応物Sodium BicarbonateHCID 516892—
溶媒DichloromethaneHCID 6344—
生成物4-Nitrophenyl 4,4,4-trifluorobutylcarbamateHCID 6658414094.6%

反応条件

温度-15 °C

反応手順

To a solution of 0.35 g (2.75 mmol) of 4,4,4-trifluoro-butylamine (CAS 819-46-5) in 20 ml of dichloromethane, cooled to −15° C., is added dropwise 1.00 g (4.96 mmol) of 4-nitrophenyl chloroformate (CAS 7693-46-1) dissolved in 15 ml of dichloromethane, while maintaining the temperature at −15° C. 0.48 ml (2.75 mmol) of diisopropylethylamine in 10 ml of dichloromethane still at −15° C. is then added. Stirring is continued at −15° C. for 45 minutes, and the temperature of the mixture is then allowed to return to 0° C. over 30 minutes. 20 ml of saturated aqueous sodium hydrogen carbonate solution are then added. The organic phase is separated out by settling and dried over sodium sulfate, and the solvent is partially evaporated off under reduced pressure to a volume of about 8 ml. This solution is chromatographed on a column of 40 g of silica gel, eluting with a mixture of 20% cyclohexane in dichloromethane, to give 0.76 g of 4-nitrophenyl 4,4,4-trifluorobutylcarbamate in the form of a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09233965B2
出典データセットuspto-grants-2016_01
ORD IDord-bee3a2e119ef41469fffe701f59b535f
出典メモuspto-grants-2016_01