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Diisobutylaluminum hydride → 4-Methoxycyclohexane-1-carbaldehyde

HRID 1488227
ノート
印刷プレビュー

反応式

HRID 1488227 の反応式
[CH3:1][O:2][CH:3]1[CH2:8][CH2:7][CH:6]([C:9](OCC)=[O:10])[CH2:5][CH2:4]1.CC(C[AlH]CC(C)C)C>ClCCl>[CH3:1][O:2][CH:3]1[CH2:8][CH2:7][CH:6]([CH:9]=[O:10])[CH2:5][CH2:4]1
参加物反応条件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 14487Diisobutylaluminum hydrideHCID 58292038Ethyl 4-methoxycyclohexane-1-carboxylate

生成物 1

HCID 2979194-Methoxycyclohexane-1-carbaldehyde

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-78 °C

実験手順

Into a 100-mL 3-neck round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of ethyl 4-methoxycyclohexane-1-carboxylate (1.3 g, 6.98 mmol) in dichloromethane (30 mL). This was followed by the addition of DIBAL-H (1 M in hexanes) (9 mL, 9 mmol) dropwise at −78° C. The reaction mixture was stirred for 3 h at −78° C., then quenched with 10 mL of NH4Cl (sat.). The aqueous phase was extracted with 3×50 mL of ethyl acetate. The combined organic layers were washed with 3×50 mL of brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. This resulted in 1 g (crude) of the title compound as a colorless oil.

後処理

  1. customInto a 100-mL 3-neck round-bottom flask purged
  2. temperaturemaintained with an inert atmosphere of nitrogen
  3. customquenched with 10 mL of NH4Cl (sat.)
  4. extractionThe aqueous phase was extracted with 3×50 mL of ethyl acetate
  5. washThe combined organic layers were washed with 3×50 mL of brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-07e98d6d615748e48a4b7c3c109671c0
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09428502B2

反応ノート

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