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Sodium Hydroxide → 1-(3,4-difluorophenyl)-1H-1,2,4-triazole-3-carboxylic acid

HRID 1755235
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HRID 1755235 반응식
[F:1][C:2]1[CH:3]=[C:4]([N:9]2[CH:13]=[N:12][C:11]([C:14]([O:16]CC)=[O:15])=[N:10]2)[CH:5]=[CH:6][C:7]=1[F:8].[OH-].[Na+]>CCO.O>[F:1][C:2]1[CH:3]=[C:4]([N:9]2[CH:13]=[N:12][C:11]([C:14]([OH:16])=[O:15])=[N:10]2)[CH:5]=[CH:6][C:7]=1[F:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 86720531ethyl 1-(3,4-difluorophenyl)-1H-1,2,4-triazole-3-carboxylate

생성물 1

HCID 867205321-(3,4-difluorophenyl)-1H-1,2,4-triazole-3-carboxylic acid수율 84%

시약·촉매·용매 1

HCID 19096565Water ethanol용매

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온도
50 °C

실험 절차

To a solution of ethyl 1-(3,4-difluorophenyl)-1H-1,2,4-triazole-3-carboxylate (0.30 g, 1.2 mmol, 1 eq) in 5 mL of EtOH/H2O (1.5:1) was added NaOH (0.095 g, 2.4 mmol, 2 eq). The reaction mixture was heated at 50° C. for 1 h then quenched with 0.20 mL of cone. HCl. The contents were filtered and washed with EtOAc then with MeOH and the MeOH filtrate was dried with Na2SO4 and concentrated in vacuo to afford 1-(3,4-difluorophenyl)-1H-1,2,4-triazole-3-carboxylic acid (0.22 g, 0.98 mmol, 84%).

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후처리

  1. customthen quenched with 0.20 mL of cone
  2. filtrationThe contents were filtered
  3. washwashed with EtOAc
  4. dry with materialwith MeOH and the MeOH filtrate was dried with Na2SO4
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9fa712c2f70249e69a6d02619310dcb7
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09169261B2

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