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Carbon Tetrachloride → 1-(Chloromethyl)-4-phenoxybenzene

HRID 77872
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반응식

HRID 77872 반응식
[O:1]([C:8]1[CH:13]=[CH:12][C:11]([CH2:14]O)=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(Cl)(Cl)(Cl)[Cl:36]>>[Cl:36][CH2:14][C:11]1[CH:12]=[CH:13][C:8]([O:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 5943Carbon TetrachlorideHCID 11776TriphenylphosphineHCID 826195(4-Phenoxyphenyl)methanol

생성물 1

HCID 5209941-(Chloromethyl)-4-phenoxybenzene수율 92%

실험 절차

To a solution of (4-phenoxy-phenyl)-methanol (408 mg, 2.04 mmol) in carbon tetrachloride (8.2 mL) was added triphenylphosphine (642 mg, 2.45 mmol) under nitrogen atmosphere at room temperature, and the reaction solution was stirred under reflux for 7 hours and 40 minutes. The reaction mixture was cooled to room temperature and concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1) to obtain the title compound (409 mg, 92%).

후처리

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temperature
under reflux for 7 hours and 40 minutes
  • concentrationconcentrated under a reduced pressure
  • customThe residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1)
  • 출처 및 근거

    ORD 기록
    ord-2670389cf36c4c69b06d1af2d077ee02
    출처 데이터셋
    uspto-grants-2014_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08841327B2

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