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Sodium Hydroxide → 1-(4-fluoro-phenyl)-5-formyl-4-isopropyl-1H-pyrazole-3-carboxylic acid

HRID 268636
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HRID 268636 반응식
C[O:2][C:3]([C:5]1[C:9]([CH:10]([CH3:12])[CH3:11])=[C:8]([CH:13]=[O:14])[N:7]([C:15]2[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=2)[N:6]=1)=[O:4].[OH-].[Na+]>CO>[F:21][C:18]1[CH:17]=[CH:16][C:15]([N:7]2[C:8]([CH:13]=[O:14])=[C:9]([CH:10]([CH3:12])[CH3:11])[C:5]([C:3]([OH:4])=[O:2])=[N:6]2)=[CH:20][CH:19]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 24754973HCID 24754973, 화합물

생성물 1

HCID 247549741-(4-fluoro-phenyl)-5-formyl-4-isopropyl-1H-pyrazole-3-carboxylic acid수율 79.2%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
60 °C

실험 절차

To a solution of 1-(4-fluoro-phenyl)-5-formyl-4-isopropyl-1H-pyrazole-3-carboxylic acid methyl ester (11.34 g, 39.1 mmol) in MeOH (150 mL) was added NaOH (156 mL of 1 N solution, 156 mmol). The reaction was heated to 60° C. for 4 hr. The solvent was then removed under reduced pressure and water (150 mL) and Et2O (100 mL) were added. The organic layer was discarded and the aqueous layer was acidified with 10% HCl to pH 1 and then extracted with EtOAc (200 mL×2). The combined organic extracts were dried over Na2SO4 and concentrated to give 1-(4-fluoro-phenyl)-5-formyl-4-isopropyl-1H-pyrazole-3-carboxylic acid (8.55 g, 79%) as a white solid that required no purification: MS(APCI+): m/z 277.0 (M+H).

후처리

  1. customThe solvent was then removed under reduced pressure and water (150 mL) and Et2O (100 mL)
  2. additionwere added
  3. extractionextracted with EtOAc (200 mL×2)
  4. dry with materialThe combined organic extracts were dried over Na2SO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-86611f2db9cf479ba8834d374198b1d9
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07446121B2

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