Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568762Generated: October 30, 2026

Acetic Anhydride → 1-Methyl-4-oxo-5-pentylcyclopent-2-en-1-yl acetate

https://huagongshe.com/reaction/568762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13137234HCID 13137234—
SolventTriethylamineHCID 8471—
Product1-Methyl-4-oxo-5-pentylcyclopent-2-en-1-yl acetateHCID 13517255—

Reaction Steps

Into the same flask as used in Example 1, dl-3-hydroxy-2-n-pentyl-3-methyl-4-cyclopentenone (18.2 g), triethylamine (0.1 g) and acetic anhydride (36 g) were charged, and the resultant mixture was stirred at 60°-80° C. for 3 hours. After completion of the reaction, the reaction mixture was subjected to the same work-up as in Example 1 to give 21.9 g of dl-3-acetoxy-2-n-pentyl-3-methyl-4-cyclopentenone. Yield, 98%. B.P., 100°-110° C./0.1-0.3 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04729953
Source datasetuspto-grants-1988_03
ORD IDord-9f45e4b61f8c422593f1fc787c080016
Source noteuspto-grants-1988_03