Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623547Generated: October 26, 2026

Hydrochloric Acid → 1-(3-(Difluoromethyl)phenyl)ethan-1-one

https://huagongshe.com/reaction/623547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant1-Bromo-3-(difluoromethyl)benzeneHCID 2769675—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product1-(3-(Difluoromethyl)phenyl)ethan-1-oneHCID 6751011998%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-bromo-3-(difluoromethyl)benzene (0.72 g, 3.48 mmol), tributyl(1-ethoxyvinyl)tin (1.38 g, 3.83 mmol), dichlorobis(triphenylphosphine)-palladium(II) (0.24 g, 0.35 mmol) in toluene (12 mL) is heated at 100° C. under nitrogen atmosphere for 16 hours. After cooling to room temperature, 2M hydrochloric acid (12 mL) is added to the mixture. Then the resulting mixture is stirred at room temperature for 1 hour. The mixture is diluted with ethyl acetate (100 mL) and washed with water (100 mL). The organic layer is dried over sodium sulfate, and concentrated under reduced pressure. The residue is purified by column chromatography on silica-gel eluting with n-hexane/ethyl acetate (30:1) to give 0.58 g (98% yield) of the title compound as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302991B2
Source datasetuspto-grants-2016_04
ORD IDord-7c6a5cf691324612944f048a01b81bdb
Source noteuspto-grants-2016_04