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Methyldichlorosilane → Dichloro(3,3-dimethylbutyl)(methyl)silane

HRID 487767
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HRID 487767 반응식
[CH2:1]=[CH:2][C:3]([CH3:6])([CH3:5])[CH3:4].[CH3:7][SiH:8]([Cl:10])[Cl:9].[SiH4]>C1COCC1.[H+].[H+].Cl[Pt-2](Cl)(Cl)(Cl)(Cl)Cl>[CH2:1]([Si:8]([CH3:7])([Cl:10])[Cl:9])[CH2:2][C:3]([CH3:6])([CH3:5])[CH3:4]
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참가 물질

6

반응물 3

HCID 6376MethyldichlorosilaneHCID 112103,3-Dimethyl-1-buteneHCID 23953Silane3회

생성물 1

HCID 19093105Dichloro(3,3-dimethylbutyl)(methyl)silane수율 93%

시약·촉매·용매 2

HCID 61859Chloroplatinic acid촉매HCID 8028Tetrahydrofuran
용매

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온도
42 °C

실험 절차

A 2 liter, 4-necked flask equipped as in Example 1 was charged with 500 g (5.94 mol) of neohexene and 1 ml of a 10% chloroplatinic acid in THF solution. The mixture was heated to reflux (about 42° C.). 805 g (5.94 mol) of methyldichlorosilane was then added dropwise. After the addition of about 70 ml of the silane, the reaction commenced and the temperature in the flask rose to 102° C. as the remainder of the silane was added. The reaction mixture was allowed to cool to room temperature (about 25° C.) after the addition of the silane. Upon completion of the reaction, the remaining volatile components were removed at reduced pressure and the residue was distilled to give 1100 g (84% of theory) of neohexylmethyldichlorosilane.

후처리

  1. customA 2 liter, 4-necked flask equipped as in Example 1
  2. temperatureThe mixture was heated
  3. additionwas added
  4. temperatureto cool to room temperature (about 25° C.)
  5. customUpon completion of the reaction
  6. customthe remaining volatile components were removed at reduced pressure
  7. distillationthe residue was distilled

출처 및 근거

ORD 기록
ord-61081ab86bd74aa48d58309b642acdf6
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05296624

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