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Toluene → 5,8-Dimethyl-2-naphthaldehyde

HRID 277172
ノート
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反応式

HRID 277172 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

20.9 g of the aldehyde compound was dissolved in 300 ml dioxane in a nitrogen atmosphere, then 50.9 g of dichlorodicyanobenzoquinone was added thereto, and the mixture was heated under reflux for 1.5 hours. After the mixture was left standing for cooling to room temperature, 500 ml toluene was added thereto, and the resulting precipitates were filtered off and washed with toluene several times. The filtrate was concentrated and the resulting crude product was purified by silica gel column chromatography to give 10.3 g of 5,8-dimethyl-2-naphthaldehyde as colorless crystals.

後処理

  1. temperaturethe mixture was heated
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
  • temperatureunder reflux for 1.5 hours
  • waitAfter the mixture was left
  • customthe resulting precipitates
  • filtrationwere filtered off
  • 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-c4a762f1436d4ef49e4b284117a06862
    出典データセット
    uspto-grants-2002_03
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06355669B1

    反応ノート

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