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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280641Generated: October 30, 2026

Ethanol → H-Lys(Z)-OL

https://huagongshe.com/reaction/1280641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTrifluoroacetic acidHCID 6422—
ReactantBoc-Lysinol(Z)HCID 10915530—
SolventWaterHCID 962—
ProductH-Lys(Z)-OLHCID 1860323368.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 4 g of benzyl (5S)-5-{[(tert-butyloxy)carbonyl]amino}-6-hydroxyhexylcarbamate, 30 cm3 of trifluoroacetic acid and 20 cm3 of ethanol is stirred at a temperature in the region of 20° C. for 2 hours. After concentration of the reaction medium under reduced pressure (5 kPa) at a temperature in the region of 40° C., the residue obtained is taken up in 50 cm3 of water and washed with twice 100 cm3 of diethyl ether. The aqueous phase is separated out after settling has taken place, basified with sodium carbonate to pH 9-10 and then extracted with 3 times 100 cm3 of dichloromethane. The combined extracts are washed with aqueous sodium chloride solution and then dried on magnesium sulphate, filtered and concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. 2.0 g of benzyl (5S)-5-amino-6-hydroxyhexylcarbamate are obtained in the form of a white solid melting at 82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451821B1
Source datasetuspto-grants-2002_09
ORD IDord-ffd9ca17134a4c01ac9520151b01c96d
Source noteuspto-grants-2002_09