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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576352Generated: October 31, 2026

Methanesulfonyl chloride → HCID 10135141, compound

https://huagongshe.com/reaction/1576352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEstradiol AcetateHCID 9818306—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 10135141HCID 10135141—

Reaction Steps

3-Acetoxy-oestra-1,3,5(10)-trien-17β-ol (500 mg., 1.6 mmole) in pyridine (2 ml.) was treated at room temperature for 16 hr. with methanesulphonyl chloride (1 ml.). The solution was diluted slowly with water (25 ml.) then the product was extracted into ether (50 ml.). The extract was washed with 2N-sulphuric acid (25 ml.) then water (50 ml.) and the solvent was evaporated in vacuo. Crystallisation of the residue from slightly aqueous methanol gave the title compound in two crops (total 519 mg., 93%), m.p. 120°-122°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03980681
Source datasetuspto-grants-1976_09
ORD IDord-3af7d9029159402aa80e9f3468a9f585
Source noteuspto-grants-1976_09