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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904353Generated: November 3, 2026

Pyridine → HCID 14326048, compound

https://huagongshe.com/reaction/1904353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 14326047HCID 14326047—
SolventHydrochloric AcidHCID 313—
ProductHCID 14326048HCID 14326048—

Reaction Steps

A mixture of the product of Step A, 5 ml of pyridine and 1 ml of methanesulfonyl chloride was stirred for 31/2 hours and was then diluted with N hydrochloric acid. The mixture was extracted with methylene chloride and the organic phase was washed with water, dried and evaporated to dryness under reduced pressure. The 677 mg of residue was chromatographed over silica and was eluted with a 7-3 mixture of hexane-ethyl acetate to obtain 410 mg of 6-(1,1-dimethylethoxy)-5-methylsulfonyloxy-4,4-dimethyl-tetrahydro-pyr-2-one melting at 64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837341
Source datasetuspto-grants-1989_06
ORD IDord-8c546283dd0643b089d49629fcef7c61
Source noteuspto-grants-1989_06