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1-Bromohexadecane → Hexadecyl(triphenyl)phosphanium bromide

HRID 634611
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HRID 634611 반응식
[C:1]1([P:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:20]([Br:36])[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35]>>[Br-:36].[CH2:35]([P+:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH3:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 82131-BromohexadecaneHCID 11776Triphenylphosphine

생성물 1

HCID 3084210Hexadecyl(triphenyl)phosphanium bromide수율 45.7%

반응 조건

온도
180 °C

실험 절차

In a 100 ml flask equipped with a stirrer, a condenser and a calcium chloride dryer tube were charged 8.6 g of triphenylphosphine and 10 g of n-hexadecyl bromide, and under nitrogen atmosphere, the mixture was heated at 180° C. for 10 hours on an oil bath. After cooling the reaction mixture to room temperature, precipitated solid material was pulverized in acetone and collected by filtration under reduced pressure. The resulting crystals were washed with acetone to obtain 8.5 g of the title compound. Melting point: 128° C.

후처리

custom
In a 100 ml flask equipped with a stirrer, a condenser and a calcium chloride dryer tube
  • temperatureAfter cooling the reaction mixture to room temperature
  • customprecipitated solid material
  • filtrationcollected by filtration under reduced pressure
  • washThe resulting crystals were washed with acetone
  • 출처 및 근거

    ORD 기록
    ord-ef9b1a08a9874b4c920fd9f3857f4664
    출처 데이터셋
    uspto-grants-2001_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06184180B2

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