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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546753Generated: November 1, 2026

Hydrochloric Acid → 4-Chloro-2-(3,4,5-trifluorophenyl)butyric acid

https://huagongshe.com/reaction/546753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Bromo-2-ChloroethaneHCID 7849—
Reactant3,4,5-Trifluorophenylacetic acidHCID 2777952—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-2-(3,4,5-trifluorophenyl)butyric acidHCID 66839530—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 2.66 M solution of butyl lithium in hexane (20 mL) was added to a solution of 3,4,5-trifluorophenylacetic acid (5.00 g) in THF (150 mL) in a nitrogen atmosphere at −78° C., and the reaction solution was stirred at −78° C. for 20 minutes. The reaction solution was further stirred at 0° C. for one hour. Then, 1-bromo-2-chloroethane (2.2 mL) was added at 0° C., and the reaction solution was stirred at room temperature for 14 hours. Ethyl acetate and 1 N hydrochloric acid were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with a saturated sodium chloride solution. The resulting organic layer was dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system) to obtain 4.54 g of the title compound. The property values of the compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935815B2
Source datasetuspto-grants-2011_05
ORD IDord-cc09b6af836e4863a155ab06c2af368a
Source noteuspto-grants-2011_05