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2,6-Difluorobenzoylisothiocyanate → HCID 13711438, 화합물

HRID 986412
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HRID 986412 반응식
[Cl:1][C:2]1[C:8]([C:9]([F:12])([F:11])[F:10])=[CH:7][C:6]([Cl:13])=[CH:5][C:3]=1[NH2:4].[F:14][C:15]1[CH:25]=[CH:24][CH:23]=[C:22]([F:26])[C:16]=1[C:17]([N:19]=[C:20]=[S:21])=[O:18]>C1C=CC=CC=1>[Cl:1][C:2]1[C:8]([C:9]([F:11])([F:10])[F:12])=[CH:7][C:6]([Cl:13])=[CH:5][C:3]=1[NH:4][C:20]([NH:19][C:17](=[O:18])[C:16]1[C:22]([F:26])=[CH:23][CH:24]=[CH:25][C:15]=1[F:14])=[S:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 109655092,6-DifluorobenzoylisothiocyanateHCID 136718552,5-Dichloro-3-(trifluoromethyl)aniline

생성물 1

HCID 13711438HCID 13711438, 화합물수율 64.3%

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

To a solution of 2,5-dichloro-3-trifluoromethylaniline (0.5 g) in 10 ml of dry benzene was added a solution of 2,6-difluorobenzoylisothiocyanate (0.45 g) in 5 ml of dry benzene under water-cooling and the solution was stirred for 10 hours. The benzene was then distilled off under reduced pressure and the residue was washed with n-hexane to obtain the desired product 0.6 g. (m.p. 136°-141° C.)

후처리

  1. temperaturecooling
  2. distillationThe benzene was then distilled off under reduced pressure
  3. washthe residue was washed with n-hexane

출처 및 근거

ORD 기록
ord-d4116d54a0244a1fb940422481a6ef78
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04713396

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