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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373987Generated: October 31, 2026

Cyclopentene → Ethyl 3-cyclopenten-1-ylbenzoate

https://huagongshe.com/reaction/1373987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopenteneHCID 8882—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-iodobenzoateHCID 143542—
CatalystTetrabutylammonium BromideHCID 74236—
SolventEthanolHCID 702—
ProductEthyl 3-cyclopenten-1-ylbenzoateHCID 12094926—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163957B2
Source datasetuspto-grants-2007_01
ORD IDord-49045b4c34f04fb9bac4eafebdc6e208
Source noteuspto-grants-2007_01