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Triphenylphosphine → HCID 178506034, 화합물

HRID 1067153
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HRID 1067153 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

To 3 l of toluene was dissolved 200.0 g (1.42 mol) of 3-fluorobromopropane, 372 g (1.42 mol) of triphenylphosphine was added thereto, and refluxed for 15 hours. Deposited crystals were filtered off and subjected to suction drying to obtain 486 g (1.21 mol) of 3-fluoropropyltriphenylphosphine bromide. Yield of this compound from 3-fluorobromopropane was 85.2%.

후처리

  • additionwas added
  • temperaturerefluxed for 15 hours
  • filtrationDeposited crystals were filtered off
  • customdrying
  • 출처 및 근거

    ORD 기록
    ord-d7973006a87c497a966e3fd56d572d6b
    출처 데이터셋
    uspto-grants-2001_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06248260B1

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