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Acetic Acid → 4-Oxocyclohexane-1-carbaldehyde

HRID 247677
ノート
印刷プレビュー

反応式

HRID 247677 の反応式
C1CO[C:3]2([CH2:8][CH2:7][C:6](=[CH:9][O:10]C)[CH2:5][CH2:4]2)[O:2]1.C(O)(=O)C>O>[CH:9]([CH:6]1[CH2:7][CH2:8][C:3](=[O:2])[CH2:4][CH2:5]1)=[O:10]
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 176Acetic AcidHCID 552771378-(Methoxymethylene)-1,4-dioxaspiro[4.5]decane

生成物 1

HCID 111709734-Oxocyclohexane-1-carbaldehyde収率 86.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

A mixture of 28.2 g of 1,1-ethylenedioxy-4-(methoxymethylene)cyclohexane, 770 ml of glacial acetic acid and 385 ml of water was heated to reflux for 1 hour in a round flask while gassing with nitrogen. Thereafter, the yellowish clear solution was cooled to room temperature, diluted with 800 ml of water and extracted three times with 700 ml of methylene chloride each time. The organic phases were washed twice with 500 ml of 10% (wt./vol.) sodium carbonate solution each time, dried over sodium sulphate, filtered and concentrated. Chromatographic separation of the brownish liquid obtained (18.5 g) on silica gel with methylene chloride as the eluent finally gave 16.7 g of 4-formylcyclohexanone as a brownish liquid.

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 1 hour in a round flask
  3. extractionextracted three times with 700 ml of methylene chloride each time
  4. washThe organic phases were washed twice with 500 ml of 10% (wt./vol.) sodium carbonate solution each time
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customChromatographic separation of the brownish liquid

出典と根拠

ORDレコード
ord-20291a54134a4fe5b3e068427ca3e505
出典データセット
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04709030

反応ノート

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