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

HRID 2408242
ノート
印刷プレビュー

反応式

HRID 2408242 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3283Diethyl EtherHCID 67332502(4E)-4-Methyl-5-(4-methylphenyl)-4-penten-1-olHCID 178418287HCID 178418287、化合物

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-8624fcc6fc074bab8f5a9aabb8512f0d
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08815792B2

反応ノート

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