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(8-Methylnaphthalen-1-yl)methanol → 8-Methyl-1-naphthaldehyde

HRID 729782
ノート
印刷プレビュー

反応式

HRID 729782 の反応式
[CH3:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10]([CH2:12][OH:13])=[CH:9][CH:8]=[CH:7]2>C(Cl)Cl>[CH3:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[C:10]([CH:12]=[O:13])=[CH:9][CH:8]=[CH:7]2
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 15618201(8-Methylnaphthalen-1-yl)methanol

生成物 1

HCID 155634878-Methyl-1-naphthaldehyde

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A 1-L 4-neck equipped with an overhead stirrer, a condenser and a thermocouple was charged with 8-methyl-1-napthalenemethanol (18.5 g, 0.107 mol) in CH2Cl2 (500 mL) and stirred at room temperature under N2. Solid Mn(IV)O2 (61 g, 0.7 mol) was carefully added and the reaction was stirred at room temperature for 3 h, then at 40° C. for 6 h and then at room temperature overnight. The reaction mixture was diluted with CH2Cl2 (500 mL), filtered and the filtrate was washed with 1N HCl and then dried over MgSO4. The resulting crude material was purified using silica gel chromatography (8/2 hexane/ethyl acetate) to yield 8-methyl-naphthalene-1-carbaldehyde as a solid.

後処理

  1. stirringthe reaction was stirred at room temperature for 3 h
このページの内容参加物実験手順後処理出典と根拠反応ノート
  • customat room temperature
  • customovernight
  • filtrationfiltered
  • washthe filtrate was washed with 1N HCl
  • dry with materialdried over MgSO4
  • customThe resulting crude material was purified
  • 出典と根拠

    ORDレコード
    ord-09c073ae4fe041d9bf7833299ec62aeb
    出典データセット
    uspto-grants-2009_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07582649B2

    反応ノート

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