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Diethyl Ether → 4-Pentenal, 4-methyl-5-(4-methylphenyl)-, (4E)-

HRID 2408242
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HRID 2408242 반응식
[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1.[CH3:12]/[C:13](=[CH:18]\[C:19]1[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=1)/[CH2:14][CH2:15][CH2:16][OH:17].C(OCC)C>ClCCl>[CH3:12]/[C:13](=[CH:18]\[C:19]1[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=1)/[CH2:14][CH2:15][CH:16]=[O:17]
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참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 67332502(4E)-4-Methyl-5-(4-methylphenyl)-4-penten-1-olHCID 178418287HCID 178418287, 화합물

생성물 1

HCID 714656444-Pentenal, 4-methyl-5-(4-methylphenyl)-, (4E)-수율 36.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Solid pyridinium chlorochromate (13.2 g, 0.06 mol) was added in one portion to a pre-cooled (−10° C.) solution of (4E)-4-Methyl-5-(4-methylphenyl)-4-penten-1-ol (9.88 g, 0.052 mol) in dry dichloromethane (250 ml) under nitrogen. After 30 minutes, the reaction was warmed up to room temperature. After 1 hour, diethyl ether (700 ml) was added to the reaction. After stirring for 10 minutes, the reaction was filtered through silica gel, rinsing with diethyl ether. The solvent was removed under vacuum and the residue was purified by column chromatography on silica gel (eluent: heptanes/ethyl acetate 10:1) followed by bulb-to-bulb distillation (100° C./0.001 mbar). 3.55 g (yield=36%) of the desired product were obtained.

후처리

  1. waitAfter 1 hour
  2. filtrationthe reaction was filtered through silica gel
  3. washrinsing with diethyl ether
  4. customThe solvent was removed under vacuum
  5. customthe residue was purified by column chromatography on silica gel (eluent: heptanes/ethyl acetate 10:1)
  6. distillationfollowed by bulb-to-bulb distillation (100° C./0.001 mbar)

출처 및 근거

ORD 기록
ord-8624fcc6fc074bab8f5a9aabb8512f0d
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815792B2

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