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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981045Generated: November 1, 2026

Pyridine → HCID 13335393, compound

https://huagongshe.com/reaction/1981045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantAcetyl chlorideHCID 6367—
Reactant4-Hydroxy-4-methyl-5-(prop-2-en-1-yl)cyclopent-2-en-1-oneHCID 12879872—
SolventWaterHCID 962—
ProductHCID 13335393HCID 1333539394.1%

Reaction Steps

Into a flask equipped with a stirrer and a thermometer, dl-2-allyl-3-hydroxy-3-methyl-4-cyclopentenone (30.4 g), pyridine (30 g) and dichloromethane (300 g) were charged, and acetyl chloride (30 g) was dropwise added thereto at a temperature from 10° to 20° C. in 2 hours. Then, stirring was continued at a room temperature for 24 hours. To the reaction mixture kept below 10° C., water (100 ml) was added to decompose excess of acetyl chloride. From the resultant mixture, the organic layer was separated and washed with 1% hydrochloric acid, 1% sodium bicarbonate solution and water in order. Removal of the solvent by distillation gave dl-3-acetoxy-2-allyl-3-methyl-4-cyclopentenone (36.5 g). Yield, 94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04511655
Source datasetuspto-grants-1985_04
ORD IDord-1dd76370304e4e2db59841bb2d7d4c34
Source noteuspto-grants-1985_04