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2-Aminothiophenol → 4-(1,3-Benzothiazol-2-yl)benzonitrile

HRID 1602034
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HRID 1602034 반응식
[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1)#[N:2].[NH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[SH:18]>CS(C)=O>[C:1]([C:3]1[CH:10]=[CH:9][C:6]([C:7]2[S:18][C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=3[N:11]=2)=[CH:5][CH:4]=1)#[N:2]
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참가 물질

4

반응물 2

HCID 87132-AminothiophenolHCID 660424-Cyanobenzaldehyde

생성물 1

HCID 15126564-(1,3-Benzothiazol-2-yl)benzonitrile

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
140 °C

실험 절차

44.6 g (0.34 mol) of 4-cyanobenzaldehyde and 54.4 g (0.64 mol) of o-aminobenzenethiol were dissolved in 300 ml of dimethyl sulfoxide, and the temperature of the solution was raised to 140° C. The produced water and the dimethyl sulfoxide were distilled off. After heating for one hr. the residue was cooled, water was added thereto, and the resultant precipitate was collected by filtration and washed with ethanol. The crude crystal thus obtained was recrystallized from ethyl acetate to give 2-(4'-cyanophenyl)benzothiazole. 22.4 g (0.095 mol) of the compound was dissolved in 250 ml of acetic acid, and 18.6 g (0.116 mol) of bromine was dropwise added thereto. As soon as bromine was added, a yellow bromine adduct was produced. Subsequently, 150 ml of water was added, and the mixture was stirred at 80° C. for 2 hr. It was then cooled, and the resultant precipitate was collected by filtration and washed with ethanol. The crude product thus obtained was recrystallized from ethyl acetate.

후처리

  1. distillationThe produced water and the dimethyl sulfoxide were distilled off
  2. temperatureAfter heating for one hr
  3. temperaturethe residue was cooled
  4. additionwater was added
  5. filtrationthe resultant precipitate was collected by filtration
  6. washwashed with ethanol
  7. customThe crude crystal thus obtained
  8. customwas recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-b3cbd3555ed04d62b35358e32a110353
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05980779

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