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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607458Generated: October 30, 2026

Methanesulfonyl chloride → HCID 131714021, compound

https://huagongshe.com/reaction/1607458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 131714017HCID 131714017—
SolventPyridineHCID 1049—
ProductHCID 131714021HCID 131714021—

Reaction Conditions

Temperature5 °C

Reaction Steps

To 1.823 g (4.15 mmole) dl-5-acetoxy-3-(3-hydroxypropyl)-2,2-dimethyl-7-(5-phenyl-2-pentyloxy)-3,4-dihydro-2H-benzopyran was added 20 ml of pyridine, the mixture stirred under nitrogen to affect solution and cooled to 5° C. Methanesulfonyl chloride, 520 mg (4.56 mmole), was added, the resulting mixture stirred at 5°-10° C. for 20 minutes, then allowed to warm to room temperature and stirred for an additional 50 minutes. The mixture was concentrated in vacuo and the residual oil taken up in ethyl acetate, washed twice with water, once with brine and the organic layer dried over anhydrous magnesium sulfate. After evaporation of solvent in vacuo the desired product was obtained as an oil, 1.999 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863934
Source datasetuspto-grants-1989_09
ORD IDord-e2d848a1119246b39499f7d4d752b31a
Source noteuspto-grants-1989_09