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

HRID 238675

반응식

HRID 238675 반응식
[Cl-].[Al+3].[Cl-].[Cl-].[F:5][C:6]([F:11])([F:10])[C:7](Cl)=[O:8].[C:12]([Cl:15])([Cl:14])=[CH2:13]>ClCCl.O>[Cl:14][C:12]([Cl:15])=[CH:13][C:7](=[O:8])[C:6]([F:11])([F:10])[F:5]

참가 물질

6

반응 조건

온도
-50 °C

실험 절차

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.

후처리

  1. customthe temperature of the reaction mixture below −30° C
  2. stirringThe reaction mixture was stirred an additional 2 h at −50° C.
  3. temperaturewarmed gradually to room temperature
  4. extractionthe aqueous layer was extracted with dichloromethane
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-47e546a997ae40af86e9cfaeef5e35a7
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08642634B2

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