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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604392Generated: November 1, 2026

4-Toluenesulfonyl chloride → Cyclobutylmethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/1604392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantCyclobutylcarbinolHCID 78130—
SolventDichloromethaneHCID 6344—
ProductCyclobutylmethyl 4-methylbenzenesulfonateHCID 13163931—

Reaction Steps

Cyclobutanemethanol(5 g, 58 mmol) was dissolved in dichloromethane (150 ml) and cooled in an ice water bath. Triethylamine (10.5 ml,-75.5 mmol) was added followed by the dropwise addition of a solution of tosyl chloride (13.3 g, 69.8 mmol) in dichloromethane (50 ml). The cooling bath was removed and the mixture allowed to warm to room temperature over 16 hours. The mixture was washed with water (2×100 ml) dried (MgSO4) and concentrated in vacuo to give cyclobutanemethanol tosylate as a yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994353
Source datasetuspto-grants-1999_11
ORD IDord-631ac6ec2d354a07b0adfcd3b1e1914d
Source noteuspto-grants-1999_11