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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132762Generated: October 26, 2026

Benzyl Bromide → Methyl 1-benzyl-2-oxocyclopentane carboxylate

https://huagongshe.com/reaction/132762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopentanecarboxylic acid, 2-oxo-, methyl esterHCID 66328—
SolventAcetoneHCID 180—
ProductMethyl 1-benzyl-2-oxocyclopentane carboxylateHCID 1084717255.1%

Reaction Steps

29.0 grams of anhydrous potassium carbonate and 132 ml of acetone were mixed, then with stirring, to the resulting mixture was dropwise added a solution of 13.0 ml of methyl 2-oxocyclopentane carboxylate in 66 ml of acetone. After stirring at room temperature for 30 minutes, 13.7 ml of benzyl bromide was dropwise added thereto, and the reaction was allowed to continue under reflux for 6 hours. Then the reaction mixture was cooled to room temperature, filtered, and concentrated, and 150 ml of toluene was added thereto. The resulting solution was washed with water (3×150 ml), dried over anhydrous sodium sulfate, concentrated, and distilled under reduced pressure. 13.4 g of colorless liquid as a distillate cut of 161-162° C./4.8 mmHg was collected. Yield: 55.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388103B2
Source datasetuspto-grants-2008_06
ORD IDord-b93bbbc2655f4f9b84ab2c4ee57aeb80
Source noteuspto-grants-2008_06