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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238675Erstellt: 24. Oktober 2026

Vinylidene chloride → 1,1,1-Trifluoro-4,4-dichloro-3-buten-2-one

https://huagongshe.com/de/reaction/238675

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVinylidene chlorideHCID 6366—
EduktTrifluoroacetyl chlorideHCID 61106—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,1,1-Trifluoro-4,4-dichloro-3-buten-2-oneHCID 15548324—

Reaktionsbedingungen

Temperatur-50 °C

Reaktionsschritte

To a solution of aluminum chloride (3.0 g, 22.5 mmol) in dichloromethane (100 mL) was added dropwise a solution of trifluoroacetyl chloride (3 g, 22.6 mmol) in dichloro-methane (5 mL) while keeping the temperature of the reaction mixture below −30° C. The reaction mixture was stirred for 15 minutes at −50° C. Then a solution of vinylidene chloride (2.2 g, 22.7 mmol) in dichloromethane (10 mL) was added dropwise over 2 h to the reaction mixture. The reaction mixture was stirred an additional 2 h at −50° C. and then warmed gradually to room temperature. The reaction mixture was diluted with water, and the aqueous layer was extracted with dichloromethane. The organic layers were combined, dried (MgSO4), and concentrated under reduced pressure to give 4,4-dichloro-1,1,1-trifluoro-3-buten-2-one as an oil which was used for the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642634B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-47e546a997ae40af86e9cfaeef5e35a7
Quellennotizuspto-grants-2014_02