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3-(2,2-Dimethoxy-ethoxy)-4'-methoxy-4-methyl-biphenyl → 4-(4-Methoxyphenyl)-7-methylbenzofuran

HRID 1372158
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반응식

HRID 1372158 반응식
CO[CH:3](OC)[CH2:4][O:5][C:6]1[CH:7]=[C:8]([C:13]2[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=2)[CH:9]=[CH:10][C:11]=1[CH3:12]>ClC1C=CC=CC=1>[CH3:20][O:19][C:16]1[CH:17]=[CH:18][C:13]([C:8]2[C:7]3[CH:3]=[CH:4][O:5][C:6]=3[C:11]([CH3:12])=[CH:10][CH:9]=2)=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 210717783-(2,2-Dimethoxy-ethoxy)-4'-methoxy-4-methyl-biphenyl

생성물 1

HCID 210717824-(4-Methoxyphenyl)-7-methylbenzofuran

시약·촉매·용매 1

HCID 7964Chlorobenzene용매2회

실험 절차

A mixture of polyphosphoric acid (approx. 0.5 g) and chlorobenzene was brought to reflux and 3-(2,2-dimethoxy-ethoxy)-4′-methoxy-4-methyl-biphenyl (1.61 g, 5.33 mmol) in chlorobenzene (12 ml) was added dropwise. After 4 h the reaction was cooled, passed through a silica plug (the plug was washed with ether), and concentrated to 1.26 g (100%) of product as a light tan solid: mp 40–41° C.; 1H NMR (300 MHz, DMSO-d6): δ 2.50 (3H, s), 3.82 (3H, s), 7.03 (1H, d, J=2.2 Hz), 7.07 (2H, d, J=9.5 Hz), 7.19 (1H, d, J=8.1 Hz), 7.23 (1H, d, J=8.1 Hz), 7.56 (2H, d, J=9.5 Hz), 8.06 (1H, d, J=2.2 Hz).

후처리

  • temperatureto reflux
  • temperatureAfter 4 h the reaction was cooled
  • washwas washed with ether), and
  • concentrationconcentrated to 1.26 g (100%) of product as a light tan solid
  • 출처 및 근거

    ORD 기록
    ord-f81764715e4246969f90d14f38bfb8dd
    출처 데이터셋
    uspto-grants-2007_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07157491B2

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