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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 20077445, 화합물

HRID 1655028
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HRID 1655028 반응식
[C:1]([CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[C:11]([O:15][CH3:16])[CH:12]=2)[C:7]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:6]1)([O:3][CH3:4])=[O:2].C(C1C(=O)C(Cl)=C(Cl)C(=O)C=1C#N)#N>C1C=CC=CC=1>[C:1]([C:5]1[N:6]=[C:7]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([O:15][CH3:16])=[CH:10][CH:9]=2)([O:3][CH3:4])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 12248098HCID 12248098, 화합물

생성물 1

HCID 20077445HCID 20077445, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A mixture of 3-carbomethoxy-6-methoxy-1-phenyl-3,4-dihydro-isoquinoline (257 mg) and DDQ (217 mg) in benzene (35 mL) was heated at reflux for 1 hr. the mixture was cooled to r.t., filtered through celite washing with toluene and the filtrate was concentrated. Flash chromatography of the residue (silica gel; toluene/EtOAc (85:15)) provided the title compound as a solid.

후처리

temperature
was heated
  • temperatureat reflux for 1 hr
  • filtrationfiltered
  • washthrough celite washing with toluene
  • concentrationthe filtrate was concentrated
  • 출처 및 근거

    ORD 기록
    ord-14e6dc37413a4f6392c74d54bb3f68b8
    출처 데이터셋
    uspto-grants-1995_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05410054

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