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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582677Generated: October 27, 2026

Hydrochloric Acid → Ethyl 3-hydroxy-3-(4'-cyclopentylphenyl)-butanoate

https://huagongshe.com/reaction/1582677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantEthyl bromoacetateHCID 7748—
Reactant1-(4-Cyclopentylphenyl)ethanoneHCID 4657913—
CatalystZincHCID 23994—
SolventBenzeneHCID 241—
ProductEthyl 3-hydroxy-3-(4'-cyclopentylphenyl)-butanoateHCID 1141471288.1%

Reaction Steps

To a refluxing mixture of 4′-cyclopentylacetophenone (17 g), I2 (5 mg) and Zn dust (12 g) in benzene (150 ml) was added ethylbromoacetate (11 ml) dropwise over 30 minutes. The mixture was refluxed for next 45 min and then cooled to room temperature. It was acidified with 10% aqueous HCl solution (150 ml) and organic layer was separated out. The organic layer was washed with water, dried (Na2SO4) and concentrated. The crude product was purified by column chromatography on silica gel to furnish 22 g (88.1% yield) of ethyl 3-hydroxy-3-(4′-cyclopentylphenyl)-butanoate (2a) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737438B2
Source datasetuspto-grants-2004_05
ORD IDord-e74bcc34dc73473797cd9abcfddfbeb0
Source noteuspto-grants-2004_05