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

HRID 1283292
ノート
印刷プレビュー

反応式

HRID 1283292 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 87132-AminothiophenolHCID 728635-Bromosalicylaldehyde

生成物 1

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

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

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%).

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
  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

出典と根拠

ORDレコード
ord-744b8c70f0294a1282161eb9dbfeb8cf
出典データセット
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03974287

反応ノート

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