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

HRID 570195
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HRID 570195 반응식
[C:1]([N:5]1[C:9]([CH3:10])=[C:8]([C:11]([O:13]C)=[O:12])[CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>CO>[C:1]([N:5]1[C:9]([CH3:10])=[C:8]([C:11]([OH:13])=[O:12])[CH:7]=[N:6]1)([CH3:4])([CH3:2])[CH3:3]
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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 acid

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate in MeOH (20 mL) was treated with 2 M aqueous NaOH solution (7.95 mL, 15.9 mmol) for 48 h at room temperature. The solvent was removed under reduced pressure and the resulting residue was dissolved in H2O (20 mL). The resulting solution was then acidified to pH-2 using 2 M HCl. The resulting precipitate was isolated by filtration, washed once with H2O (20 mL), and the solid was dried under high vacuum to yield 1-tert-Butyl-5-methyl-1H-pyrazole-4-carboxylic acid. 1H-NMR (400 MHz, d6-DMSO) δ: 12.16 (br. s., 1H), 7.67 (s, 1H), 2.69 (s, 3H), 1.59 (s, 9H).

후처리

  1. customThe solvent was removed under reduced pressure
  2. dissolutionthe resulting residue was dissolved in H2O (20 mL)
  3. customThe resulting precipitate was isolated by filtration
  4. washwashed once with H2O (20 mL)
  5. customthe solid was dried under high vacuum

출처 및 근거

ORD 기록
ord-99b13e4ea58a47aaa73b96a568823942
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09023846B2

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