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2-Aminothiophenol → 2-(Benzo[d]thiazol-2-yl)-4-bromophenol

HRID 329250
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HRID 329250 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[SH:8].[Br:9][C:10]1[CH:17]=[C:14]([CH:15]=O)[C:13]([OH:18])=[CH:12][CH:11]=1>N1C=CC=CC=1>[OH:18][C:13]1[CH:12]=[CH:11][C:10]([Br:9])=[CH:17][C:14]=1[C:15]1[S:8][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[N:1]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 87132-AminothiophenolHCID 728635-Bromosalicylaldehyde

생성물 1

HCID 2420572-(Benzo[d]thiazol-2-yl)-4-bromophenol

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

2-Aminothiophenol (12.5 g, 0.1 mole) was dissolved in 30 ml. of pyridine and 20.1 g (0.1 mole) of 5-bromosalicylaldehyde was added dropwise during 15 minutes. The solution was warmed on a steam bath for 2 hours and then a stream of air was bubbled through the mixture while heating for another hour. The mixture was poured into 300 ml. of 2 N HCl which was then stirred until crystals formed. The product was removed by filtration, washed with water and recrystallized from ethanol, mp. 164°-165°. Yield, 8.0 g. (26%).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperatureThe solution was warmed on a steam bath for 2 hours
  2. customa stream of air was bubbled through the mixture
  3. temperaturewhile heating for another hour
  4. additionThe mixture was poured into 300 ml
  5. customformed
  6. customThe product was removed by filtration
  7. washwashed with water
  8. customrecrystallized from ethanol, mp. 164°-165°
  9. customYield

출처 및 근거

ORD 기록
ord-ab81c0adf6814dc5b08a9a02c489b5c3
출처 데이터셋
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04020165

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