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3-Methyl-2-butanone → 1-(4-Fluorophenyl)-4-methylpent-1-en-3-one

HRID 2295233
ノート
印刷プレビュー

反応式

HRID 2295233 の反応式
[O-]CC.[Na+].[CH3:5][C:6]([CH:8]([CH3:10])[CH3:9])=[O:7].[F:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=O)=[CH:14][CH:13]=1>C(O)C.CCOCC>[F:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=[CH:5][C:6](=[O:7])[CH:8]([CH3:10])[CH3:9])=[CH:14][CH:13]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 112513-Methyl-2-butanoneHCID 680234-FluorobenzaldehydeHCID 2723922Sodium ethoxide

生成物 1

HCID 537214671-(4-Fluorophenyl)-4-methylpent-1-en-3-one収率 53%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 3283Diethyl Ether溶媒

実験手順

A sodium ethoxide solution (21% by weight in EtOH, 4.86 gm, 15 mmol) was added to a mixture of methylisopropylketone (8.61 gm, 100 mmol, from Aldrich) and 4-fluorobenzaldehyde (12.411 gm, 100 mmol, from Aldrich) in ethanol (150 ml). The solution was allowed to stir at room temperature for 3 hours. The solvent was evaporated to afford an orange oil. The oil was dissolved in ether, washed with saturated NH4Cl and brine, then dried over Na2SO4, filtered and concentrated to give an orange oil. The oil was purified by distillation (bp=106° C. at 1.3 mm Hg) to afford the title compound as a pale yellow oil (10.118 gm, 53%).

後処理

  1. customThe solvent was evaporated
  2. customto afford an orange oil
  3. washwashed with saturated NH4Cl and brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give an orange oil
  8. distillationThe oil was purified by distillation (bp=106° C. at 1.3 mm Hg)

出典と根拠

ORDレコード
ord-4df04c3c130041ac8b818c3b4ba00e6d
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05691322

反応ノート

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