Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546754Generated: October 30, 2026

Oxalyl chloride → 4-Chloro-2-(3,4,5-trifluorophenyl)butyryl chloride

https://huagongshe.com/reaction/546754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-Chloro-2-(3,4,5-trifluorophenyl)butyric acidHCID 66839530—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-Chloro-2-(3,4,5-trifluorophenyl)butyryl chlorideHCID 86615146—

Reaction Steps

oxalyl chloride (0.63 mL) and DMF (1 drop) were added to a solution of 4-chloro-2-(3,4,5-trifluorophenyl)butyric acid (1.17 g) in methylene chloride (30 mL) at 0° C., and the reaction solution was stirred at room temperature for one hour. The reaction solution was concentrated under reduced pressure to obtain 4-chloro-2-(3,4,5-trifluorophenyl)butyric acid chloride. A solution of 4-chloro-2-(3,4,5-trifluorophenyl)butyric acid chloride in THF (5 mL) was added to a solution of tert-butyl carboxylate (600 mg) and triethylamine (3.1 mL) in THF (20 mL) at 0° C., and the reaction solution was stirred at room temperature for one hour. The reaction solution was added to a saturated sodium bicarbonate solution, followed by extraction with ethyl acetate. The resulting extract 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 1.35 g of the title compound. The property value of the compound is as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935815B2
Source datasetuspto-grants-2011_05
ORD IDord-0fa48b748a064e00880ca494e898a306
Source noteuspto-grants-2011_05