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Triphenylphosphine → HCID 178506034, 화합물

HRID 1941025
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HRID 1941025 반응식
[F:1][CH2:2][CH2:3][CH2:4][Br:5].[C:6]1([P:12]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>C1(C)C=CC=CC=1>[Br-:5].[F:1][CH2:2][CH2:3][CH2:4][PH:12]([C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1)([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11776TriphenylphosphineHCID 67699Propane, 1-bromo-3-fluoro-

생성물 1

HCID 178506034HCID 178506034, 화합물수율 85.2%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

3-Fluorobromopropane (200.0 g, 1.42 mol) was dissolved in toluene (3), followed by adding to the solution, triphenylphosphine (37.2 g, 1.42 mol), refluxing the mixture for 15 hours, filtering off the resulting product, and suction-drying, to obtain 3-fluoropropyltriphenylphosphine bromide (486 g, 1.21 mol). Yield: 85.2%.

후처리

  1. temperature
refluxing the mixture for 15 hours
  • filtrationfiltering off the resulting product
  • customsuction-drying
  • 출처 및 근거

    ORD 기록
    ord-e4e6cd7fe3bc460b9acc0cf9d888fa4a
    출처 데이터셋
    uspto-grants-1997_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05702641

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