Propylethinylcarbinol → 5-(1-Hydroxybutyl)-3-phenylisoxazole

HRID 1613869

반응식

HRID 1613869 반응식
[CH:1](=[N:8][OH:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:10]#[C:11][CH:12]([OH:16])[CH2:13][CH2:14][CH3:15].Cl[O-].[Na+]>ClCCl>[OH:16][CH:12]([C:11]1[O:9][N:8]=[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH:10]=1)[CH2:13][CH2:14][CH3:15]

참가 물질

5

반응물 3

HCID 7746PropylethinylcarbinolHCID 12143(Z)-Benzaldehyde oximeHCID 23665760Sodium Hypochlorite

생성물 1

HCID 108893475-(1-Hydroxybutyl)-3-phenylisoxazole

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

In 25 ml of dichloromethane, were dissolved 5.0 g (41.3 mmol) of benzaldoxime and 4.5 g (45.9 mmol) of 1-hexyne-3-ol. Under ice cooling, 29.0 g of a 12.0% aqueous solution of sodium hypochlorite were added dropwise to the solution over 30 minutes. After completion of the dropwise addition, they were reacted at 20° C. for 2 hours. After completion of the reaction, the reaction mixture was extracted with dichloromethane and the organic layer was washed with water. The organic layer was dried over anhydrous sodium sulfate and the solvent was then distilled off under reduced pressure. The residue was purified by chromatography on a silica gel column (eluent: chloroform), whereby the target compound, namely, 5-(1-hydroxybutyl)-3-phenylisooxazole was obtained as an oil.

후처리

  1. additionAfter completion of the dropwise addition, they
  2. customwere reacted at 20° C. for 2 hours
  3. customAfter completion of the reaction
  4. extractionthe reaction mixture was extracted with dichloromethane
  5. washthe organic layer was washed with water
  6. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  7. distillationthe solvent was then distilled off under reduced pressure
  8. customThe residue was purified by chromatography on a silica gel column (eluent: chloroform), whereby the target compound

출처 및 근거

ORD 기록
ord-4ad035274a71409e80554c84d11358e9
출처 데이터셋
uspto-grants-1993_03
특허 번호
US05194606

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