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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779359Generated: October 31, 2026

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

https://huagongshe.com/reaction/1779359

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 numberUS05627174
Source datasetuspto-grants-1997_05
ORD IDord-6a8f564b24b243d08c72eba3eef27947
Source noteuspto-grants-1997_05