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2-(2-Hydroxy-2-phenylethoxy)benzene-1,4-diol → 2,3-Dihydro-2-phenyl-benzo[1,4]dioxin-6-ol

HRID 1455022
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HRID 1455022 반응식
O[CH:2]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH2:3][O:4][C:5]1[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:6]=1[OH:12]>C1(C)C=CC=CC=1>[C:13]1([CH:2]2[O:12][C:6]3[CH:7]=[CH:8][C:9]([OH:11])=[CH:10][C:5]=3[O:4][CH2:3]2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
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참가 물질

3

반응물 1

HCID 179786042-(2-Hydroxy-2-phenylethoxy)benzene-1,4-diol

생성물 1

HCID 179785732,3-Dihydro-2-phenyl-benzo[1,4]dioxin-6-ol

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of 2-(2-hydroxy-2-phenylethoxy)benzene-1,4-diol (1.2 g) in toluene (75 ml) was heated with Amberlyst 15 catalyst (0.5 g) under reflux for 7 hrs. After filtering the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (toluene/ethyl acetate/acetic acid, 8:1:1). The yield of 2,3-dihydro-2-phenyl-benzo[1,4]dioxin-6-ol is 0.5 g. 1H NMR (DMSO-d6) δ: 4.02 (dd, J 8.5, 11.4 Hz, 1H), 4.35 (dd, J 2.3, 11.4 Hz, 1H), 5.11 (dd, J 8.5, 2.3 Hz, 1H), 6.29 (dd, J 2.8, 8.5 Hz, 1H), 6.32 (d, J 2.8 Hz, 1H), 6.75 (d, J 8.5 Hz, 1H), 7.36-7.47 (m, 5H), 8.99 (s, 1H).

후처리

  1. temperatureunder reflux for 7 hrs
  • filtrationAfter filtering the solvent
  • customwas evaporated under reduced pressure
  • customThe residue was purified by column chromatography on silica gel (toluene/ethyl acetate/acetic acid, 8:1:1)
  • 출처 및 근거

    ORD 기록
    ord-05e92f0d64c54675a8e3a9eb16fd8ea6
    출처 데이터셋
    uspto-grants-2009_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07482340B2

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