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Sodium Hydroxide → 2-Bromothiazole-5-carboxylic acid

HRID 372186
ノート
印刷プレビュー

反応式

HRID 372186 の反応式
[Br:1][C:2]1[S:3][C:4]([C:7]([O:9]C)=[O:8])=[CH:5][N:6]=1.[OH-].[Na+]>CO>[Br:1][C:2]1[S:3][C:4]([C:7]([OH:9])=[O:8])=[CH:5][N:6]=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 14798Sodium HydroxideHCID 2773502Methyl 2-bromothiazole-5-carboxylate

生成物 1

HCID 27632102-Bromothiazole-5-carboxylic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture containing 10 g. of 2-bromo-5-methoxycarbonylthiazole, 100 ml. of 10% aqueous sodium hydroxide and 200 ml. of methanol is stirred at 0° C for 5 minutes. The methanol is distilled off in vacuo and the resulting concentrate extracted twice with ethyl acetate. The remaining aqueous phase is acidified by the careful addition of dilute aqueous hydrochloric acid resulting in the formation of a precipitate which is then recovered by filtration and dried under vacuum yielding 2-bromo-5-carboxythiazole.

後処理

  1. additionA mixture containing 10 g
  2. distillationThe methanol is distilled off in vacuo
  3. concentrationthe resulting concentrate
  4. extractionextracted twice with ethyl acetate
  5. additionThe remaining aqueous phase is acidified by the careful addition of dilute aqueous hydrochloric acid resulting in the formation of a precipitate which
  6. filtrationis then recovered by filtration
  7. customdried under vacuum

出典と根拠

ORDレコード
ord-88dc2156b4c1436ba9bdcaf5319c1528
出典データセット
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04089865

反応ノート

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