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Toluene → 5,8-Dimethyl-2-naphthaldehyde

HRID 1384068
ノート
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反応式

HRID 1384068 の反応式
ClC1[C:7](=[O:8])[C:6]([C:9]#N)=[C:5](C#N)[C:4](=O)C=1Cl.[C:15]1([CH3:21])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.O1CCOC[CH2:23]1>>[CH3:21][C:15]1[CH:20]=[CH:19][C:18]([CH3:23])=[C:17]2[C:16]=1[CH:4]=[CH:5][C:6]([CH:7]=[O:8])=[CH:9]2
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 3

HCID 1140TolueneHCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 312751,4-Dioxane

生成物 1

HCID 144876095,8-Dimethyl-2-naphthaldehyde

実験手順

In a nitrogen atmosphere, the obtained aldehyde (20.9 g) was dissolved in dioxane (300 ml). After adding dichlorodicyanobenzoquinone (50.9 g), the resultant mixture was heated under ref lux for 1.5 hr. Then, it was cooled to room temperature by allowing to stand followed by the addition of toluene (500 ml). The resulting precipitate was collected by filtration and washed with toluene several times. The filtrate was concentrated and the resulting crude product was purified by silica gel column chromatography to give 5,8-dimethyl-2-naphtaldehyde (10.3 g) as colorless crystals.

後処理

  1. filtrationThe resulting precipitate was collected by filtration
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
  • washwashed with toluene several times
  • concentrationThe filtrate was concentrated
  • customthe resulting crude product was purified by silica gel column chromatography
  • 出典と根拠

    ORDレコード
    ord-6294218e16c246ea8157c401ff11b926
    出典データセット
    uspto-grants-2001_07
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06258811B1

    反応ノート

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