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Sodium Hydroxide → 4-(Trifluoromethyl)Thiazole-5-Carboxylic Acid

HRID 389088
ノート
印刷プレビュー

反応式

HRID 389088 の反応式
[OH-].[Na+].[F:3][C:4]([F:16])([F:15])[C:5]1[N:6]=[CH:7][S:8][C:9]=1[C:10]([O:12]CC)=[O:11]>C(O)C>[F:16][C:4]([F:3])([F:15])[C:5]1[N:6]=[CH:7][S:8][C:9]=1[C:10]([OH:12])=[O:11]
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 135933995-Thiazolecarboxylic acid, 4-(trifluoromethyl)-, ethyl ester

生成物 1

HCID 189433734-(Trifluoromethyl)Thiazole-5-Carboxylic Acid収率 99.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

An aqueous sodium hydroxide solution (2 ml) was added to a solution of ethyl 4-(trifluoromethyl)-1,3-thiazole-5-carboxylate (301 mg) in ethanol (3 ml), followed by stirring at room temperature for 4 hours. The reaction solution was concentrated under reduced pressure and water was added thereto, followed by washing with diethylether. A 1M hydrochloric acid (2 ml) was added to the aqueous layer, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure to obtain 4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acid (261 mg) as a light brown solid.

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

後処理

  1. concentrationThe reaction solution was concentrated under reduced pressure and water
  2. additionwas added
  3. washby washing with diethylether
  4. additionA 1M hydrochloric acid (2 ml) was added to the aqueous layer
  5. extractionfollowed by extraction with ethyl acetate
  6. washThe organic layer was washed with saturated brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-901215f9323249abad37b22f8e7bd8ca
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08377923B2

反応ノート

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