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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cyclopentanecarboxylic acid, 2-oxo-, methyl ester | HCID 66328 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 1-benzyl-2-oxocyclopentane carboxylate | HCID 10847172 | 55.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07388103B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-b93bbbc2655f4f9b84ab2c4ee57aeb80 |
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| Source note | uspto-grants-2008_06 |
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