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Sodium Hydroxide → 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylic acid

HRID 12868
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HRID 12868 반응식
C[O:2][C:3]([C:5]1[CH:6]=[N:7][N:8]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:9]=1[CH3:10])=[O:4].[OH-].[Na+]>CO>[C:11]([N:8]1[C:9]([CH3:10])=[C:5]([C:3]([OH:4])=[O:2])[CH:6]=[N:7]1)([CH3:14])([CH3:12])[CH3:13]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 50853230Methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate

생성물 1

HCID 222279031-tert-butyl-5-methyl-1H-pyrazole-4-carboxylic acid수율 78%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
25 °C

실험 절차

A solution of 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylic acid methyl ester (2.0 g, 10.19 mmol) in methanol (6.8 mL) cooled to 0° C. was treated dropwise with a 4N aqueous sodium hydroxide solution (5.1 mL, 20.4 mmol). The reaction was allowed to slowly warm to 25° C. The reaction was stirred at 25° C. overnight. At this time, the reaction was concentrated in vacuo to remove methanol. The residue was diluted with water (25 mL) and was then extracted with ethyl acetate (1×25 mL). The aqueous layer was then acidified to pH=1 with a 3N aqueous hydrochloric acid solution. The resulting precipitate was collected by filtration, washed with water and hexanes, and then dried in vacuo to afford 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylic acid (1.43 g, 78%) as a white solid.

후처리

  1. concentrationAt this time, the reaction was concentrated in vacuo
  2. customto remove methanol
  3. additionThe residue was diluted with water (25 mL)
  4. extractionwas then extracted with ethyl acetate (1×25 mL)
  5. filtrationThe resulting precipitate was collected by filtration
  6. washwashed with water and hexanes
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-0b6c02ce31c94ea9abd81308aa4bb6b6
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728029B2

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