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O-Xylene → 1,1,4,4,6,7-Hexamethyl-1,2,3,4-tetrahydronaphthalene

HRID 277180
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HRID 277180 반응식
[Cl-].[Al+3].[Cl-].[Cl-].Cl[C:6]([CH3:14])([CH2:8][CH2:9][C:10](Cl)([CH3:12])[CH3:11])[CH3:7].[C:15]1([CH3:22])[C:16]([CH3:21])=[CH:17][CH:18]=[CH:19][CH:20]=1>>[CH3:22][C:15]1[C:16]([CH3:21])=[CH:17][C:18]2[C:10]([CH3:12])([CH3:11])[CH2:9][CH2:8][C:6]([CH3:14])([CH3:7])[C:19]=2[CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7237O-XyleneHCID 80360Hexane, 2,5-dichloro-2,5-dimethyl-HCID 6451240Aluminum(III) Chloride

생성물 1

HCID 2276411,1,4,4,6,7-Hexamethyl-1,2,3,4-tetrahydronaphthalene

실험 절차

7 g of aluminum chloride was added by portions to 200 ml solution of 50 g 2,5-dichloro-2,5-dimethylhexane in orthoxylene at 0° C. under stirring. After the mixture was stirred at the same temperature for 15 minutes, it was poured into ice-cold water and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and then evaporated to give 60 g of 2,3,5,5,8,8-hexamethyl-5,6,7,8-tetrahydronaphthalene as a brown oil.

후처리

  1. stirringAfter the mixture was stirred at the same temperature for 15 minutes
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • additionit was poured into ice-cold water
  • extractionextracted with ethyl acetate
  • washThe organic layer was washed with brine
  • dry with materialdried over anhydrous magnesium sulfate
  • customevaporated
  • 출처 및 근거

    ORD 기록
    ord-776ba37bdddb44b9bc5c5baf68b6c105
    출처 데이터셋
    uspto-grants-2002_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06355669B1

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