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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701474Generated: October 30, 2026

Chloride → HCID 57294516, compound

https://huagongshe.com/reaction/1701474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20341182HCID 20341182—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 57294516HCID 57294516—

Reaction Steps

To a solution of 1hydroxy-8a-methyl-1-vinyl-1,2,6,7,8,8a-hexahydro-6-naphthalenone (0.204 g.) in anhydrous methylene chloride (20 ml.) was added 0.5 ml. of pyridine. The reaction mixture was cooled in an ice-bath and thionyl chloride (150 mg.) was added. After 5 minutes, the reaction mixture was diluted with methylene chloride (20 ml.) and water (10 ml.) and neutralized with saturated sodium bicarbonate solution (5 ml.). The aqueous layer was extracted with methylene chloride (3×25 ml.) and the combined organic layers were washed with brine and dried over sodium sulfate. Evaporation of solvent gave 217 mg. of the oily chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04193878
Source datasetuspto-grants-1980_03
ORD IDord-ef5243f61ef94febb54d549067187076
Source noteuspto-grants-1980_03