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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613364Generated: November 3, 2026

Benzyl Alcohol → benzyl N-(chlorosulfonyl)carbamate

https://huagongshe.com/reaction/1613364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantChlorosulfonyl isocyanateHCID 70918—
SolventDichloromethaneHCID 6344—
Productbenzyl N-(chlorosulfonyl)carbamateHCID 1494713688.1%

Reaction Steps

To a solution of 43.5 ml (0.5 mole) of chlorosulfonyl isocyanate in 400 ml of methylene chloride, stirred in an ice bath, was added 51.6 ml (0.5 mole) of benzyl alcohol over an one hr period. The reaction mixture was concentrated under reduced pressure and the solid residue was triturated in petroleum ether (bp range 35°-65° C.). The solid was collected by filtration, rinsed twice with petroleum ether and dried under vacuum to give 110 g (88% yield) of benzyloxycarbonylsulfamoyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192785
Source datasetuspto-grants-1993_03
ORD IDord-0b82cd3df8f143b49281b44ee049432a
Source noteuspto-grants-1993_03