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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432229Generated: October 30, 2026

Methanesulfonyl chloride → HCID 22346726, compound

https://huagongshe.com/reaction/432229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 15272330HCID 15272330—
SolventPyridineHCID 1049—
ProductHCID 22346726HCID 2234672672%

Reaction Steps

A solution of 3-propylidene-1-cyclobutanol (0.344 g, 0.00307 mol) in pyridine (5 mL) was cooled to 0° C. Methanesulfonyl chloride (0.422 g, 0.00369 mol) was added dropwise, keeping the temperature below 2° C. The mixture was stirred for two hours, and then poured into ice water (15 mL) and extracted with ethyl ether (2×10 mL). The combined organic layers were washed with water (3×10 mL). The organic layer was dried over magnesium sulfate and the solvent was removed in vacuo to give 3-propylidenecyclobutyl methanesulfonate (0.492 g, 0.00221 mol) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-e711d40093ac4cf1a06859d95c8f86c1
Source noteuspto-grants-2003_12