Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629975Generated: October 30, 2026

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

https://huagongshe.com/reaction/1629975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant4,4,4-TrifluorobutylamineHCID 136645—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product4-Nitrophenyl 4,4,4-trifluorobutylcarbamateHCID 6658414094.6%

Reaction Conditions

Temperature-15 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791119B2
Source datasetuspto-grants-2014_07
ORD IDord-0346689324cb42a1b0581b8878f50f9d
Source noteuspto-grants-2014_07