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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108676Generated: October 31, 2026

Benzyl chloroformate → 2-Benzyloxycarbonylamino-4-methoxycarbonylphenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1108676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant2-Amino-4-methoxycarbonylphenyl trifluoromethanesulfonateHCID 14493069—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product2-Benzyloxycarbonylamino-4-methoxycarbonylphenyl trifluoromethanesulfonateHCID 22627443—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 2-amino-4-methoxycarbonylphenyl trifluoromethanesulfonate (2.6 g) in a mixture of pyridine (5.6 ml) and dichloromethane (20 ml) was added benzyl chloroformate (2.08 ml) at 0° C., and the mixture was stirred at 20° C. for 4.5 hours. The mixture was diluted with dichloromethane and washed successively with diluted hydrochloric acid, aqueous sodium bicarbonate and brine. The organic layer was dried over sodium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel eluting with dichloromethane to give 2-benzyloxycarbonylamino-4-methoxycarbonylphenyl trifluoromethanesulfonate (2.61 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069156
Source datasetuspto-grants-2000_05
ORD IDord-7c7873db9e3d4c059e5a71acc54e1d00
Source noteuspto-grants-2000_05