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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375994Generated: October 25, 2026

Methyl formate → 3-Oxo-cyclopentanecarboxylic acid methyl ester

https://huagongshe.com/reaction/375994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
ReactantTrimethyl orthoformateHCID 9005—
Reactant3-Oxocyclopentanecarboxylic acidHCID 227798—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product3-Oxo-cyclopentanecarboxylic acid methyl esterHCID 237640—

Reaction Conditions

Temperature10 °C

Reaction Steps

318.36 g (3 mol) of trimethylorthoformate are added gradually to a solution of 128.2 g (1 mol) of nonracemic 3-oxocyclopentanecarboxylic acid and 11.4 g (0.06 mol) of p-toluene sulfonic acid hydrate in 380 ml of methanol within 5-10 minutes while stirring, The mixture is heated and during 25 minutes a mixture of formic acid methyl ester and methanol is distilled off (about 185 g of distillate), Thereafter 29 g of 30% sodium methylate solution (0.16 mol) are added and the reaction mixture is kept boiling under reflux for 2 hours; methanol is distilled off, the residue cooled to 10° C. and dissolved by adding 230 ml of methylene chloride and 200 ml of water. By adding 5% sulfuric acid the mixture is adjusted to pH 1.4 and stirred at 10° C. for 30 minutes. The methylene chloride phase is separated and the aqueous phase extracted again with 100 ml of methylene chloride. The combined organic phases are stirred with 50 ml of water, separated and the solvent is distilled off in vacuo. The residue is fractionated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488136
Source datasetuspto-grants-1996_01
ORD IDord-c7e2963c623b4c9b8cea55662fcbef8f
Source noteuspto-grants-1996_01