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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355516Generated: October 26, 2026

4-Nitrophenyl chloroformate → (S)-4-nitrophenyl 2-(t-butoxycarbonylamino)-3-cyclohexylpropylcarbamate

https://huagongshe.com/reaction/2355516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantSodium BicarbonateHCID 516892—
Reactant(S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamateHCID 10988904—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-nitrophenyl 2-(t-butoxycarbonylamino)-3-cyclohexylpropylcarbamateHCID 5938296767%

Reaction Steps

To a stirred solution of (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate (0.65 g, 2.54 mmol) in MeCN (20 mL) and THF (5 mL) was added powdered NaHCO3 (0.43 g, 5.08 mmol) followed by a solution of p-nitrophenyl chloroformate (0.51 g, 5.08 mmol) in MeCN (20 mL) dropwise over 10 min. The mixture was stirred at rt for 2 h, filtered through a pad of Celite and concentrated to leave a white solid. This material was purified by chromatography on a 40-g silica cartridge eluted with a gradient from 0-100% EtOAc in hexanes to afford (S)-tert-butyl 1-(p-nitrophenoxycarbonylamino)-3-cyclohexylpropan-2-ylcarbamate (0.67 g, 67%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-fdce4cf4a2284b30a7efc8e26edc286e
Source noteuspto-grants-2010_07