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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352Generated: October 26, 2026

Water → 1-Phenylcyclopentanecarboxylic acid

https://huagongshe.com/reaction/1352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-DibromobutaneHCID 8056—
ReactantPhenylacetonitrileHCID 8794—
ReactantEthyl AcetateHCID 8857—
SolventTetrahydrofuranHCID 8028—
SolventSodium hydrideHCID 24758—
Product1-Phenylcyclopentanecarboxylic acidHCID 66167—

Reaction Steps

In a stream of argon, 60% sodium hydride was dissolved in 10 ml of tetrahydrofuran, and the solution was mixed with 2.0 g of benzyl cyanide, stirred for 1 hour at room temperature, further mixed with 3.69 g of 1,4-dibromobutane and again stirred for 16 hours at room temperature. The reaction mixture was mixed with water and ethyl acetate, and the resulting organic layer was separated, washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. After removing the solvent by distillation under a reduced pressure, the thus obtained residue was subjected to silica gel column chromatography, and the resulting hexane eluate was mixed with 45 ml of sulfuric acid and subjected to 24 hours of heating under reflux. After cooling down to room temperature, the reaction solution was mixed with ice water and ethyl acetate to separate water layer which was subsequently mixed with concentrated hydrochloric acid and ethyl acetate, and the resulting organic layer was separated, washed with water and a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. By removing the solvent by distillation under a reduced pressure, 978 mg of 1-phenylcyclopentanecarboxylic acid was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723606
Source datasetuspto-grants-1998_03
ORD IDord-d699a2fd0bfb49f2b2d9d51a6a3e6ab2
Source noteuspto-grants-1998_03