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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032506Generated: November 2, 2026

Methyl iodide → Methyl 7-(4-hydroxycyclopent-2-en-1-on-2-yl)-5-heptynoate

https://huagongshe.com/reaction/1032506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant7-(4-Hydroxycyclopent-2-en-1-on-2-yl)-5-heptynoic acidHCID 14774425—
SolventAcetoneHCID 180—
ProductMethyl 7-(4-hydroxycyclopent-2-en-1-on-2-yl)-5-heptynoateHCID 1465622581.4%

Reaction Steps

A stirred mixture of 5.8 g of 7-(4-hydroxycyclopent-2-en-1-on-2-yl)-5-heptynoic acid, 3.95 g of potassium carbonate, 7.4 g of iodomethane and 52 ml of acetone was refluxed for 2.5 hours. Most of the acetone was evaporated and the residue was partitioned with water and ether. The ether layer was separated, washed with brine, dried and concentrated, giving 5.02 g of the desired compound as an oil; PMR δ 3.72 (3H, s, methyl ester).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04958037
Source datasetuspto-grants-1990_09
ORD IDord-24863c94644649c4bc1e57ddfd25ad83
Source noteuspto-grants-1990_09