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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 623547Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/623547

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Edukt1-Bromo-3-(difluoromethyl)benzeneHCID 2769675—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(3-(Difluoromethyl)phenyl)ethan-1-oneHCID 6751011998%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09302991B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-7c6a5cf691324612944f048a01b81bdb
Quellennotizuspto-grants-2016_04