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Methyl p-toluenesulfonate → HCID 20430720, 화합물

HRID 2413319
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HRID 2413319 반응식
[C:1]1([Sb: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.[C:20]1([CH3:31])[CH:25]=[CH:24][C:23]([S:26]([O:29]C)(=[O:28])=[O:27])=[CH:22][CH:21]=1>>[C:20]1([CH3:31])[CH:21]=[CH:22][C:23]([S:26]([O-:29])(=[O:27])=[O:28])=[CH:24][CH:25]=1.[CH3:20][Sb+: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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6645Methyl p-toluenesulfonateHCID 11777Triphenylantimony

생성물 1

HCID 20430720HCID 20430720, 화합물

반응 조건

온도
130 °C

실험 절차

A mixture of 17.65 g (0.05 mol) of triphenylstibine and 9.31 g (0.05 mol) of methyl p-toluenesulfonate was heated in a 130° C. bath with nitrogen bubbling through the melt for 18 hr. The resulting syrup was cooled to an amorphous glass which was crystallized by treatment with ether. The resultant crystals were collected and dried.

후처리

  1. temperatureThe resulting syrup was cooled to an amorphous glass which
  2. customwas crystallized by treatment with ether
  3. customThe resultant crystals were collected
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-8320cbeb6e56435d802eb3c8adb0e549
    출처 데이터셋
    uspto-grants-1985_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04496643

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