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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726131Generated: October 31, 2026

3,4,4-Trifluoro-3-butenoyl chloride → HCID 21836481, compound

https://huagongshe.com/reaction/726131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,4-Trifluoro-3-butenoyl chlorideHCID 10920789—
ReactantHCID 178418336HCID 178418336—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
ProductHCID 21836481HCID 21836481—

Reaction Steps

To a solution of 3,4,4-trifluoro-3-butenoyl chloride (3.75 g, 23.65 mmol) in anhyd. ether (100 mL) was treated with copper(I)iodide (2.28 g, 12 mmol) followed by 24 mL of 1.0M solution of benzylmagnesium chloride in ether dropwise at -78° C. with stirring under nitrogen. The reaction mixture was stirred at -78° C. for 10 min and allowed to reach to r.t. and filtered. The filtrate was successively washed with 2N HCl, 5% sodium bicarbonate and brine, and dried. The residue, a mixture of several products, obtained after evaporation of the solvent was chromatographed over silica gel (20% hexanes in dichloromethane) and the major product (least polar) was isolated and further purified by kugelrohr distillation, b.p. 130°-140° C. (pot temperature)/12 mmHg. Proton and fluorine NMR spectra of this material was found to correspond to the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708032
Source datasetuspto-grants-1998_01
ORD IDord-f590fd2e2f56437d9d582472148ef8c4
Source noteuspto-grants-1998_01