HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373987Generated: October 31, 2026
Cyclopentene → Ethyl 3-cyclopenten-1-ylbenzoate
https://huagongshe.com/reaction/1373987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentene | HCID 8882 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-iodobenzoate | HCID 143542 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-cyclopenten-1-ylbenzoate | HCID 12094926 | — |
Reaction Steps
The following are successively introduced into a round-bottomed flask: 7 g of ethyl 3-iodobenzoate (25 mmol), 11.2 ml of cyclopentene (127 mmol), 21 ml of ethanol, 1.16 g of Pd2 dba3 complex (1.27 mmol), 8.8 g of potassium carbonate (63 mmol) and 8.17 g of nBu4NBr (25 mmol). The medium is heated at 80° C. for 16 hours and then the black mixture is filtered on celite. The precipitate is washed with ethyl acetate. The filtrate is washed with water and then with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and then concentrated under reduced pressure. The title product, which is isolated by bulb to bulb distillation (5.2 g), is obtained in the form of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163957B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-49045b4c34f04fb9bac4eafebdc6e208 |
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| Source note | uspto-grants-2007_01 |
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