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Benzaldehyde → 1-Hydroxy-2-methyl-1-phenyl-3-pentanone

HRID 22060
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HRID 22060 반응식
[CH:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:9]([C:11]([CH2:13][CH3:14])=[O:12])[CH3:10]>>[C:2]1([CH:1]([OH:8])[CH:9]([CH3:10])[C:11](=[O:12])[CH2:13][CH3:14])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 240BenzaldehydeHCID 7288Ethyl ketone

생성물 1

HCID 5460171-Hydroxy-2-methyl-1-phenyl-3-pentanone수율 72%

반응 조건

온도
-78 °C

실험 절차

50 mmol (5.1 ml) of benzaldehyde are added at -78° C. to the manganous enolate of diethyl ketone, prepared by the procedure described above. After stirring for 10 seconds at -78° C., the reaction medium is hydroIyzed by the dropwise addition of a saturated solution of (NH4)2SO4. After decantation, filtration on hyflo-supercel and evaporation of the solvents under vacuum, 5-phenyl-5-hydroxy-4-methylpentan-3-one is isolated by low pressure liquid chromatography on 15 μm silica gel using cyclohexane/ethyl acetate (90/10) as the eluent. Yield=72%. Erythro/threo=61/39.

후처리

  1. customprepared by the procedure
  2. filtration
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
After decantation, filtration
  • customon hyflo-supercel and evaporation of the solvents under vacuum
  • 출처 및 근거

    ORD 기록
    ord-eb2ffed42db34070991af4f46a60fd88
    출처 데이터셋
    uspto-grants-1995_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05426201

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