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Toluene → 5,8-Dimethyl-2-naphthaldehyde

HRID 277172
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HRID 277172 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

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

생성물 1

HCID 144876095,8-Dimethyl-2-naphthaldehyde

실험 절차

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.

후처리

  1. temperaturethe mixture was heated
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • 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
  • 출처 및 근거

    ORD 기록
    ord-c4a762f1436d4ef49e4b284117a06862
    출처 데이터셋
    uspto-grants-2002_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06355669B1

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