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Potassium Hydroxide → 2,3-dihydro-2,4-dimethyl-3-phenyl-7-crotyloxy-1H-inden-1-one

HRID 4994
ノート
印刷プレビュー

反応式

HRID 4994 の反応式
[CH3:1][CH:2]1[CH:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:9]2[C:4](=[C:5]([OH:18])[CH:6]=[CH:7][C:8]=2[CH3:17])[C:3]1=[O:19].[CH2:20](Br)[CH:21]=[CH:22][CH3:23].[OH-].[K+]>CC(C)=O>[CH3:1][CH:2]1[CH:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:9]2[C:4](=[C:5]([O:18][CH2:20][CH:21]=[CH:22][CH3:23])[CH:6]=[CH:7][C:8]=2[CH3:17])[C:3]1=[O:19]
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 14797Potassium HydroxideHCID 1224142-Butene, 1-bromo-HCID 148347312,3-dihydro-2,4-dimethyl-3-phenyl-7-hydroxy-1H-inden-1-one

生成物 1

HCID 540414322,3-dihydro-2,4-dimethyl-3-phenyl-7-crotyloxy-1H-inden-1-one

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A solution of 19.0 g of 2,3-dihydro-2,4-dimethyl-3-phenyl-7-hydroxy-1H-inden-1-one, 13.98 of crotyl bromide and 5.47 g of potassium hydroxide in 200 ml of acetone was heated and refluxed under stirring condition. After the reaction was completed, the reaction mixture was concentrated and extracted with ethyl acetate, then the extract was washed with water and with an aqueous solution saturated with sodium chloride, then dried. The extract was concentrated by removing the solvent under a reduced pressure, then recrystallized from methanol to obtain 11.8 g of 2,3-dihydro-2,4-dimethyl-3-phenyl-7-crotyloxy-1H-inden-1-one as in the form of cis-trans mixture. Colorless stick-like crystals. Melting point: 138.5°-139.5° C.

後処理

  1. temperaturerefluxed
  2. concentrationthe reaction mixture was concentrated
  3. extractionextracted with ethyl acetate
  4. washthe extract was washed with water and with an aqueous solution saturated with sodium chloride
  5. customdried
  6. concentrationThe extract was concentrated
  7. customby removing the solvent under a reduced pressure
  8. customrecrystallized from methanol

出典と根拠

ORDレコード
ord-052823d5aace48c1ba767bdcf24f3608
出典データセット
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05242919

反応ノート

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