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Triphenylphosphine → Hexyltriphenylphosphonium iodide

HRID 2399128
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HRID 2399128 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.[I:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]>C1(C)C(C)=CC=CC=1>[I-:20].[CH2:21]([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)[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11776TriphenylphosphineHCID 125271-Iodohexane

생성물 1

HCID 10994370Hexyltriphenylphosphonium iodide수율 93.9%

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

A mixture of 28.82 g of triphenylphosphine, 21.2 g of 1-iodo-hexane and 200 ml of xylene was refluxed for 5 hours and then was cooled. The solvent was decanted and the gummy residue was triturated with ether and dried at 90° to 100° C. under reduced pressure to obtain 44.53 g of n-hexyltriphenylphosphonium iodide melting at 106° C.

후처리

temperature
was refluxed for 5 hours
  • temperaturewas cooled
  • customThe solvent was decanted
  • customthe gummy residue was triturated with ether
  • customdried at 90° to 100° C. under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-6258c4f0ba694f10987cebffac7094b4
    출처 데이터셋
    uspto-grants-1977_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04027040

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