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Nitric Acid → 3-tert-butyl-4-nitro-1H-pyrazole-5-carboxylic acid

HRID 1063801
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HRID 1063801 반응식
[C:1]([C:5]1[NH:9][N:8]=[C:7]([C:10]([OH:12])=[O:11])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].S(=O)(=O)(O)O.[N+:18]([O-])([OH:20])=[O:19]>>[C:1]([C:5]1[NH:9][N:8]=[C:7]([C:10]([OH:12])=[O:11])[C:6]=1[N+:18]([O-:20])=[O:19])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

4

반응물 3

HCID 944Nitric AcidHCID 1118Sulfuric AcidHCID 20680393-tert-butyl-1H-pyrazole-5-carboxylic acid

생성물 1

HCID 222774293-tert-butyl-4-nitro-1H-pyrazole-5-carboxylic acid

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온도
60 °C

실험 절차

5-tert-Butyl-1H-pyrazol-3-carboxylic acid (5 g, 29.7 mmol) was added portionwise to concentrated sulfuric acid (25 ml) at room temperature with stirring. The reaction mixture was then heated to 60° C. and concentrated nitric acid (70%, 5.15 ml) was added dropwise, keeping the temperature at 60° C. The reaction was then stirred at 60° C. for 2.5 hours, cooled to room temperature and poured onto 50 ml of ice with stirring. After 15 minutes the white precipitate was isolated by filtration, washed with water and dried under reduced pressure to give 5-tert-butyl-4-nitro-1H-pyrazol-3-carboxylic acid (6.0 g) as a white solid. 1H NMR (400 MHz, DMSO-D6): δ=13.50-13.88 (2H, brs), 1.13 (9H, s) ppm. LRMS (electrospray): m/z [M+Na]+ 236, [M−H]+ 212.

후처리

  1. customat 60° C
  2. stirringThe reaction was then stirred at 60° C. for 2.5 hours
  3. temperaturecooled to room temperature
  4. stirringwith stirring
  5. customAfter 15 minutes the white precipitate was isolated by filtration
  6. washwashed with water
  7. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-323a61cf6d78447e813171759d9ce03e
출처 데이터셋
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06967204B2

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