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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265173Generated: October 26, 2026

Triphenylphosphine → 3-Oxo-cyclopentanecarboxylic acid methyl ester

https://huagongshe.com/reaction/1265173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantOzoneHCID 24823—
ReactantMethyl 3-methylidenecyclopentane-1-carboxylateHCID 557110—
SolventDichloromethaneHCID 6344—
Product3-Oxo-cyclopentanecarboxylic acid methyl esterHCID 23764054%

Reaction Steps

A solution of methyl 3-methylenecyclopentane carboxylate (Trost, B. M., Chan, M. T., J. Am. Chem. Soc., 1983, 105, 2315) (2.84 g, 20.26 mmol) in dichloromethane (60 mL) was cooled to −78° C. and a slow stream of ozone was passed through until the permanent blue color indicated complete ozonide formation. The excess ozone was purged with stream of nitrogen. Triphenylphosphine (10.62 g, 40.52 mmol) was added, and stirring was continued overnight, allowing the temperature to warm up to ambient. Solvent was removed in vacuo, the residue dissolved in 10 mL of ethyl acetate/hexane (1:4) mixture. The crystalline triphenylphosphine oxide was removed by filtration, and the residue was purified by mplc (ethyl acetate/hexanes (1:4) to yield 1.5651 g (54%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545023B2
Source datasetuspto-grants-2003_04
ORD IDord-614990dbe74b4f5a94ab46b9806897b9
Source noteuspto-grants-2003_04