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Sodium Hydroxide → HCID 57652715, 화합물

HRID 1013267
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HRID 1013267 반응식
C[O:2][C:3]([C:5]1[CH:6]=[C:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[O:22][CH3:23])[CH:8]=[C:9]([N:11]2[CH:15]=[N:14][N:13]=[N:12]2)[CH:10]=1)=[O:4].[OH-].[Na+]>CO>[CH3:23][O:22][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=1[C:7]1[CH:8]=[C:9]([N:11]2[CH:15]=[N:14][N:13]=[N:12]2)[CH:10]=[C:5]([C:3]([OH:4])=[O:2])[CH:6]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 57652729HCID 57652729, 화합물

생성물 1

HCID 57652715HCID 57652715, 화합물수율 51.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 2′-methoxy-5-tetrazol-1-yl-biphenyl-3-carboxylic acid methyl ester (8.6 g, 27.7 mmol), 3N aqueous NaOH (28.5 mL) and MeOH (28.5 mL) was stirred at room temperature for 18 hours. The reaction mixture was filtered and the collected solid was partitioned between 1N aqueous HCl and methylene chloride. A white precipitate formed in the methylene chloride layer and was collected by filtration, washed with water and methylene chloride, and dried to give 4.2 g (46%) of 2′-methoxy-5-tetrazol-1-yl-biphenyl-3-carboxylic acid, MP=214.0-215.3° C., MS (M+H)=297.

후처리

  1. filtrationThe reaction mixture was filtered
  2. customthe collected solid was partitioned between 1N aqueous HCl and methylene chloride
  3. customA white precipitate formed in the methylene chloride layer
  4. filtrationwas collected by filtration
  5. washwashed with water and methylene chloride
  6. customdried

출처 및 근거

ORD 기록
ord-3c7619e294f04665802dbb69ae431d05
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981914B2

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