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Sodium Hydroxide → 4-{[(4-Biphenylyloxy)acetyl]amino}-3-thiophenecarboxylic acid

HRID 14593
ノート
印刷プレビュー

反応式

HRID 14593 の反応式
C[O:2][C:3]([C:5]1[C:9]([NH:10][C:11](=[O:26])[CH2:12][O:13][C:14]2[CH:19]=[CH:18][C:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[CH:16][CH:15]=2)=[CH:8][S:7][CH:6]=1)=[O:4].[OH-].[Na+]>C(O)C>[C:17]1([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:16]=[CH:15][C:14]([O:13][CH2:12][C:11]([NH:10][C:9]2[C:5]([C:3]([OH:4])=[O:2])=[CH:6][S:7][CH:8]=2)=[O:26])=[CH:19][CH:18]=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 24886422Methyl 4-{[(4-biphenylyloxy)acetyl]amino}-3-thiophenecarboxylate

生成物 1

HCID 117031034-{[(4-Biphenylyloxy)acetyl]amino}-3-thiophenecarboxylic acid収率 104.9%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To 4-[2-(biphenyl-4-yloxy)-acetylamino]-thiophene-3-carboxylic acid methyl ester (100 mg, 0.259 mmol) in ethanol (6 mL) was added a solution of sodium hydroxide (1N, 0.41 mL, 0.41 mmol) and the reaction was stirred at room temperature for 30 hours. After such time the reaction mixture was filtered through glass wool and the filtrate was then neutralized by addition of a solution of hydrochloric acid (1N, 0.39 mL). The precipitate was filtered, washed with water and dried in vacuo to yield the title compound as a white solid (96 mg, 80%).

後処理

  1. filtrationAfter such time the reaction mixture was filtered through glass wool
  2. additionthe filtrate was then neutralized by addition of a solution of hydrochloric acid (1N, 0.39 mL)
  3. filtrationThe precipitate was filtered
  4. washwashed with water
  5. customdried in vacuo

出典と根拠

ORDレコード
ord-625a92c473c249fa9b471dd4bd97d822
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07732452B2

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