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Phenyl Isothiocyanate → 5-Chloro-N-phenyl-1,3-benzodithiol-2-imine

HRID 2419551
노트
인쇄 미리보기

반응식

HRID 2419551 반응식
[C:1]1([N:7]=[C:8]=[S:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:10][C:11]1[CH:12]=[CH:13][C:14]2[S:18]N=N[C:15]=2[CH:19]=1>>[Cl:10][C:11]1[CH:12]=[CH:13][C:14]2[S:18][C:8](=[N:7][C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[S:9][C:15]=2[CH:19]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7673Phenyl IsothiocyanateHCID 124949945-Chlorobenzo[d][1,2,3]thiadiazole

생성물 1

HCID 203138485-Chloro-N-phenyl-1,3-benzodithiol-2-imine수율 24.6%

반응 조건

온도
220 °C

실험 절차

Phenylisothiocyanate (8.8g) and 5-chloro-1,2,3-benzothiadiazole (3.75g) are combined under an inert atmosphere and heated at 220° C until nitrogen evolution ceases. Initial purification of the product is accomplished by dry column chromatography (600g alumina column, benzene solvent). The product is further purified with a methylene chloride wash and recrystallization (twice) from pentane to yield 1.5g of the title compound, melting point 71°-73° C.

후처리

  1. customInitial purification of the product
  2. dry with materialby dry column chromatography (600g alumina column, benzene solvent)
  3. customThe product is further purified with a methylene chloride
  4. washwash
  5. customrecrystallization (twice) from pentane

출처 및 근거

ORD 기록
ord-4a3ee462bb3d4e3585c441a3b603fcb3
출처 데이터셋
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04107175

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