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

HRID 14593
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HRID 14593 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 24886422Methyl 4-{[(4-biphenylyloxy)acetyl]amino}-3-thiophenecarboxylate

생성물 1

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

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-625a92c473c249fa9b471dd4bd97d822
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732452B2

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