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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 1-(4-fluorophenyl)-3-methyl-1H-pyrazole-4-carboxylic acid

HRID 1744469
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반응식

HRID 1744469 반응식
O.[F:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH:13]=[C:12]([C:14]([O:16]CC)=[O:15])[C:11]([CH3:19])=[N:10]2)=[CH:5][CH:4]=1.[OH-].[Na+]>C(O)C>[F:2][C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH:13]=[C:12]([C:14]([OH:16])=[O:15])[C:11]([CH3:19])=[N:10]2)=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 22228060Ethyl 1-(4-fluorophenyl)-3-methylpyrazole-4-carboxylate

생성물 1

HCID 222280571-(4-fluorophenyl)-3-methyl-1H-pyrazole-4-carboxylic acid

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

To a mixed solvent of ethanol (40 ml) and water (40 ml) were added ethyl 1-(4-fluorophenyl)-3-methylpyrazole-4-carboxylate (8.5 g) and sodium hydroxide (1.66 g), and the mixture was stirred at a refluxing temperature for 2 h. After the reaction, ethanol was evaporated and to the residue was added dilute hydrochloric acid. The obtained solid was recrystallized from aqueous methanol solution to give the title compound, melting point: 194–195° C.

후처리

  1. customwas evaporated and to the residue
  2. additionwas added dilute hydrochloric acid
  3. customThe obtained solid was recrystallized from aqueous methanol solution

출처 및 근거

ORD 기록
ord-acb36e67ecfe48ac937268c9f2f5f074
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07015218B1

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