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1-(5,5-Dimethylcyclohex-1-en-1-yl)ethan-1-one → HCID 20569421、化合物

HRID 746366
ノート
印刷プレビュー

反応式

HRID 746366 の反応式
[CH3:1][C:2]([C:4]1[CH2:9][C:8]([CH3:11])([CH3:10])[CH2:7][CH2:6][CH:5]=1)=[O:3].[H-].[H-].[H-].[H-].[Li+].[Al+3]>CCOCC>[CH3:1][CH:2]([OH:3])[C:4]1[CH2:9][C:8]([CH3:11])([CH3:10])[CH2:7][CH2:6][CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 126685191-(5,5-Dimethylcyclohex-1-en-1-yl)ethan-1-oneHCID 21226445Aluminium lithium hydride

生成物 1

HCID 20569421HCID 20569421、化合物収率 85%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

A solution of 1-(5′,5′-dimethylcyclohex-1′-enyl)ethanone (13.1 g, 85.8 mmol) in Et2O (50 ml) was added dropwise with stirring within 50 min. to a suspension of LAH (895 mg, 23.6 mmol) in Et2O (150 ml). The reaction mixture was refluxed for 1 h prior to quenching at 0° C. by careful addition of water (50 ml) followed by 5 N aq. HCl (50 ml). The organic layer was separated and the aqueous one extracted with Et2O. The combined ethereal solutions were washed with water and brine, dried (Na2SO4), and concentrated in a rotary evaporator. Silica-gel FC (pentane/Et2O, 9:1, Rf=0.14) of the resulting residue (14.7 g) gave 11.2 g (85%) of 1-(5′,5′-dimethylcyclohex-1′-enyl)ethanol.

後処理

  1. temperatureThe reaction mixture was refluxed for 1 h
  2. customto quenching at 0° C. by careful addition of water (50 ml)
  3. customThe organic layer was separated
  4. extractionthe aqueous one extracted with Et2O
  5. washThe combined ethereal solutions were washed with water and brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated in a rotary evaporator

出典と根拠

ORDレコード
ord-aaf271fcf2e345e0aff63f8e9b08bf0c
出典データセット
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07393822B2

反応ノート

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