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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112093Generated: October 31, 2026

4-Toluenesulfonyl chloride → Tert-butyl (3-tosyl-cyclobutyl)-carbamate

https://huagongshe.com/reaction/2112093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl (3-hydroxycyclobutyl)carbamateHCID 22594430—
SolventChloroformHCID 6212—
ProductTert-butyl (3-tosyl-cyclobutyl)-carbamateHCID 86606183—

Reaction Steps

18.7 g (100 mmol) tert.butyl (3-hydroxy-cyclobutyl)-carbamate and 12.1 g (120 mmol) triethylamine are placed in 500 ml chloroform. 20.5 g (105 mmol) tosyl chloride, dissolved in 150 ml chloroform, is added dropwise to this solution at 0° C. with stirring. Then the mixture is left to come up to ambient temperature and stirred for 2 h. The organic phase is washed successively with water, dilute hydrochloric acid, sodium hydrogen carbonate solution and water. The organic phase is dried with magnesium sulphate and the solvent is eliminated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521457B2
Source datasetuspto-grants-2009_04
ORD IDord-772b9e55fe9a428abf4d39157259cee8
Source noteuspto-grants-2009_04