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Methyldichlorosilane → Silane, dichloro(3-chloro-2-methylpropyl)methyl-

HRID 65500
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[SiH:1]([Cl:4])([Cl:3])[Cl:2].[CH2:5]([Cl:9])[C:6](=[CH2:8])[CH3:7].[CH3:10][SiH:11]([Cl:13])[Cl:12]>>[CH3:10][Si:11]([CH2:8][CH:6]([CH2:5][Cl:9])[CH3:7])([Cl:13])[Cl:12].[Si:1]([CH2:7][CH:6]([CH2:5][Cl:9])[CH3:8])([Cl:4])([Cl:3])[Cl:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6376MethyldichlorosilaneHCID 112413-Chloro-2-methyl-1-propeneHCID 24811Trichlorosilane

생성물 2

HCID 86664Silane, trichloro(3-chloro-2-methylpropyl)-수율 21.5%HCID 102659Silane, dichloro(3-chloro-2-methylpropyl)methyl-수율 68.8%

실험 절차

In a 100 ml apparatus, there as combined 13.6 g (0.1 mol) of Cl3SiH, 9.1 g (0.1 mol) of methallyl chloride, and 11.5 g (0.1 mol) of MeSiHCl2, followed by 0.05 ml Pt catalyst solution at 21° C. Gentle heating caused an exothermic reaction to 52° C. in 22 min. The complete reaction was vacuum distilled, yielding 14.14 g (68.8%) of MeSiCl2CH2CHMeCH2Cl and 4.86 g (21.5%) of Cl3SiCH2CHMeCH2Cl. This example indicates that at the equimolar level, neither Cl3SiH nor MeSiHCl2 is an effective promoter for reactions of the other with methallyl chloride.

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후처리

  1. temperatureGentle heating
  2. customan exothermic reaction to 52° C. in 22 min
  3. customThe complete reaction
  4. distillationdistilled

출처 및 근거

ORD 기록
ord-c12899d85d1249d1b179e11e3daa130e
출처 데이터셋
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04614812

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