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Hydrochloric Acid → 2-Amino-5-(4-hydroxyphenylthio)thiazole

HRID 2380620
ノート
印刷プレビュー

反応式

HRID 2380620 の反応式
C([NH:4][C:5]1[S:6][C:7]([S:10][C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)=[CH:8][N:9]=1)(=O)C.Cl>C(O)C>[NH2:4][C:5]1[S:6][C:7]([S:10][C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)=[CH:8][N:9]=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 313Hydrochloric AcidHCID 157291802-Acetylamino-5-(4-hydroxyphenylthio)thiazole

生成物 1

HCID 157291812-Amino-5-(4-hydroxyphenylthio)thiazole収率 84%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of 2-acetylamino-5-(4-hydroxyphenylthio)thiazole (1.5 g) in a mixture of ethanol (40 ml) and aqueous 6N hydrochloric acid (6 ml) was refluxed for 4.5 hours with stirring. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in water. The solution was adjusted to pH 10 using aqueous sodium hydroxide under ice cooling. The precipitates were collected by filtration and recrystallized from a mixture of ethanol and water (3:1) to give 2-amino-5-(4-hydroxyphenylthio)thiazole (1.05 g, yield: 84.0%).

後処理

  1. temperaturewas refluxed for 4.5 hours
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. dissolutionthe residue was dissolved in water
  4. filtrationThe precipitates were collected by filtration
  5. customrecrystallized from a mixture of ethanol and water (3:1)

出典と根拠

ORDレコード
ord-d6100dc3f8ad408ba52ee675dcb84b3a
出典データセット
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05369107

反応ノート

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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