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HRID 589836作成日:2026年10月26日

Diisopropylethylamine → 4-Nitrophenyl 1,1,1-trifluoro-2-methylpropan-2-ylcarbamate

https://huagongshe.com/reaction/589836

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Sodium BicarbonateHCID 516892—
反応物1,1,1-Trifluoro-2-methylpropan-2-amineHCID 11275188—
溶媒DichloromethaneHCID 6344—
生成物4-Nitrophenyl 1,1,1-trifluoro-2-methylpropan-2-ylcarbamateHCID 6658410126.1%

反応条件

温度-15 °C

反応手順

To a solution of 0.35 g (2.75 mmol) of 1,1,1-trifluoro-2-methylpropan-2-ylamine (CAS 812-18-0) 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 is then added, still at −15° C. Stirring is continued at −15° C. for 2 hours, and the temperature of the mixture is then allowed to return to 0° C. over 1 hour. 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 0.21 g of 4-nitrophenyl 1,1,1-trifluoro-2-methylpropan-2-ylcarbamate 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-fc3b6c7a4e284c7db39ca0f8a09d666f
出典メモuspto-grants-2016_01