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Dichloromethane → Methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate

HRID 12867
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HRID 12867 반응식
[CH3:1][O:2][C:3](=[O:12])[C:4](=[CH:8]N(C)C)[C:5](=O)[CH3:6].Cl.[C:14]([NH:18][NH2:19])([CH3:17])([CH3:16])[CH3:15].C([O-])(=O)C.[Na+].ClCCl>C(O)C>[CH3:1][O:2][C:3]([C:4]1[CH:8]=[N:19][N:18]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:5]=1[CH3:6])=[O:12]
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참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 81889tert-Butylhydrazine monohydrochlorideHCID 517045Sodium AcetateHCID 53395488Methyl 2-((dimethylamino)methylene)-3-oxobutanoate

생성물 1

HCID 50853230Methyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate수율 71%

시약·촉매·용매 1

HCID 702
Ethanol
용매

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온도
90 °C

실험 절차

A solution of 2-dimethylaminomethylene-3-oxo-butyric acid methyl ester (7.43 g, 43.40 mmol) in absolute ethanol (70 mL) was treated with tert-butylhydrazine hydrochloride (5.52 g, 44.29 mmol) and sodium acetate (4.42 g, 53.88 mmol). The resulting mixture was heated to 90° C. for 18 h. At this time, the reaction was cooled to 25° C. The reaction was poured onto ice using dichloromethane to assist the transfer (50 mL). The mixture was transferred to a separatory funnel at which time the layers were shaken and separated. The aqueous layer was further extracted with dichloromethane (1×50 mL). The combined organics were washed with a saturated aqueous sodium bicarbonate solution (1×50 mL), water (1×50 mL) and a saturated aqueous sodium chloride solution (1×50 mL), dried over magnesium sulfate, filtered and concentrated in vacuo. ISCO CombiFlash (120 g column; 0-10% ethyl acetate/hexanes) afforded 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylic acid methyl ester (6.04 g, 71%) as a yellow oil.

후처리

  1. temperatureAt this time, the reaction was cooled to 25° C
  2. additionThe reaction was poured onto ice
  3. customThe mixture was transferred to a separatory funnel at which time
  4. customseparated
  5. extractionThe aqueous layer was further extracted with dichloromethane (1×50 mL)
  6. washThe combined organics were washed with a saturated aqueous sodium bicarbonate solution (1×50 mL), water (1×50 mL)
  7. dry with materiala saturated aqueous sodium chloride solution (1×50 mL), dried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-5c72efe1e923436eb6ffc65c2c606b2c
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728029B2

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