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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629981Generated: October 25, 2026

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

https://huagongshe.com/reaction/1629981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantSodium BicarbonateHCID 516892—
Reactant1,1,1-Trifluoro-2-methylpropan-2-amineHCID 11275188—
SolventDichloromethaneHCID 6344—
Product4-Nitrophenyl 1,1,1-trifluoro-2-methylpropan-2-ylcarbamateHCID 6658410126.1%

Reaction Conditions

Temperature-15 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791119B2
Source datasetuspto-grants-2014_07
ORD IDord-72ceb5bc7a2249f686eb0c909eb45dc8
Source noteuspto-grants-2014_07