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Ethyl Acetate → HCID 59574725, 화합물

HRID 2092054
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HRID 2092054 반응식
[CH3:1][Si:2]([CH3:16])([CH3:15])[CH2:3][CH2:4][O:5][CH2:6][N:7]1[CH:11]=[C:10]([C:12](=[O:14])[CH3:13])[CH:9]=[N:8]1.[BH4-].[Na+].C(OCC)(=O)C>CO>[CH3:15][Si:2]([CH3:1])([CH3:16])[CH2:3][CH2:4][O:5][CH2:6][N:7]1[CH:11]=[C:10]([CH:12]([OH:14])[CH3:13])[CH:9]=[N:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8857Ethyl AcetateHCID 4311764Sodium borohydrideHCID 595743441-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-4-yl)ethanone

생성물 1

HCID 59574725HCID 59574725, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1-(1-{[2-(Trimethylsilyl)ethoxy]methyl}-1H-pyrazol-4-yl)ethanone (39.7 mg, 0.17 mmol) in methanol (2 mL) was mixed with sodium borohydride (12.5 mg, 0.34 mmol) and stirred at room temperature for 90 minutes. After completion of the reaction, the reaction solution was mixed with ethyl acetate and washed with saturated aqueous sodium chloride. The organic layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure. The resulting crude reaction product containing the desired product was used for the next step (43.7 mg).

후처리

  1. customAfter completion of the reaction
  2. washwashed with saturated aqueous sodium chloride
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. customevaporated under reduced pressure
  5. customThe resulting crude reaction product

출처 및 근거

ORD 기록
ord-fa028201fb1044b3b60fecf7d9743192
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08440666B2

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