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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235674Generated: October 26, 2026

Diazomethane → 3-Oxo-cyclopentanecarboxylic acid methyl ester

https://huagongshe.com/reaction/235674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
Reactant3-Oxocyclopentanecarboxylic acidHCID 227798—
SolventDiethyl EtherHCID 3283—
Product3-Oxo-cyclopentanecarboxylic acid methyl esterHCID 237640—

Reaction Steps

To a solution of 2.8 g of 3-oxocyclopentanecarboxylic acid in 20 ml of diethyl ether was added ethereal solution of diazomethane under cooled with ice until the mixture turned pale yellow, and then the reaction mixture was concentrated under reduced pressure to give about 3.1 g of 3-oxocyclopentanecarboxylic acid methyl ester as crude product. Obtained methyl ester compound was dissolved in 20 ml of methanol and after the mixture was cooled to -50° C., 820 mg of sodium borohydride was added thereto at a time and the mixture was stirred for 20 minutes at the same temperature. After 1.3 ml of acetic acid was dropped slowly to the reaction mixture, methanol was removed under reduced pressure. To the residue was added 10 ml of water and the mixture was extracted with ethyl acetate and the extract was washed successively with water and a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 3 g of the title compound as crude product having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04640931
Source datasetuspto-grants-1987_02
ORD IDord-abc81155c82f4b41ab51fd67f03d0ce3
Source noteuspto-grants-1987_02