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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772679Generated: October 27, 2026

4-Toluenesulfonyl chloride → Ethyl 3-(tosyloxy)cyclobutane-1-carboxylate

https://huagongshe.com/reaction/1772679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantEthyl 3-hydroxycyclobutane-1-carboxylateHCID 21716982—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(tosyloxy)cyclobutane-1-carboxylateHCID 57478426—

Reaction Steps

To a solution of ethyl 3-hydroxycyclobutanecarboxylate (10.2 g, 78.4 mmol) in dry pyridine (56.5 mL) at 0° C., TsCl (14.9 g, 78.4 mmol) was added portionwise. The resulting mixture was stirred at rt overnight. The reaction mixture was concentrated under reduced pressure and the residue obtained was dissolved in EtOAc (100 mL) and sequentially washed with 2 N HCl (100 mL), saturated NaHCO3 (100 mL) and water (100 mL). The EtOAc layer was dried over Na2SO4, filtered, and concentrated to obtain ethyl 3-(tosyloxy)cyclobutanecarboxylate as a pale yellow oil, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249163B2
Source datasetuspto-grants-2016_02
ORD IDord-94c4518beadd41b28b79976728de0385
Source noteuspto-grants-2016_02