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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252225Generated: October 25, 2026

Triethylamine → 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol

https://huagongshe.com/reaction/1252225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acidHCID 13334384—
SolventTetrahydrofuranHCID 8028—
Product4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanolHCID 20140800—

Reaction Steps

To a mixture of 4-methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid (14.0 g) and triethylamine (5.25 g) in tetrahydrofuran (280 ml), ethyl chloroformate (5.64 g) was added with ice-cooling and then stirred for 30 minutes. The resulting triethylamine hydrochloride was removed by filtration. To filtrate was added sodium borohydride (5 g) in water (90 mg) with ice-cooling, and the mixture was stirred for 1.5 hours. The reaction mixture was concentrated to a volume of 120 ml in vacuo and extracted with dichloromethane. The dichloromethane layer was washed with diluted hydrochloric acid and then water, dried over anhydrous sodium sulfate and evaporated in vacuo to give an oily residue which was then purified by silica gel chromatography to give 4-methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742052
Source datasetuspto-grants-1988_05
ORD IDord-aeb5bb4dba7b42c5bfeaebee6c17486c
Source noteuspto-grants-1988_05