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Thionyl Chloride → 3-Difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl chloride

HRID 1440100
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HRID 1440100 반응식
S(Cl)([Cl:3])=O.[F:5][CH:6]([F:23])[O:7][C:8]1[C:9]([F:22])=[C:10]([C:14]([N+:19]([O-:21])=[O:20])=[C:15]([F:18])[C:16]=1[F:17])[C:11](O)=[O:12]>C1C=CC=CC=1>[F:5][CH:6]([F:23])[O:7][C:8]1[C:9]([F:22])=[C:10]([C:14]([N+:19]([O-:21])=[O:20])=[C:15]([F:18])[C:16]=1[F:17])[C:11]([Cl:3])=[O:12]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 150238363-(Difluoromethoxy)-2,4,5-trifluoro-6-nitrobenzoic acid

생성물 1

HCID 150238423-Difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl chloride

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

40 ml of thionyl chloride were added to a solution of 15.97 g (0.056 moles) of 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoic acid [(XII), R1 =--OCHF2, R3' =NO2, X=X'=F] in 50 ml of benzene, and the mixture was heated under reflux for 2 hours. At the end of this time, the benzene and the excess thionyl chloride were removed by distillation under reduced pressure to give 16.50 g of 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl chloride [(XIII), R1 =--OCHF2, R3' =NO2, X=X'=F].

후처리

  1. temperatureunder reflux for 2 hours
  2. customAt the end of this time, the benzene and the excess thionyl chloride were removed by distillation under reduced pressure

출처 및 근거

ORD 기록
ord-26adc1dc920e49baac13270d1e4fcbf5
출처 데이터셋
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05496951

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