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3,3,3-Trifluoropropyltrichlorosilane → Silane, dichlorobis[3,3,3-trifluoropropyl]-

HRID 2226975
ノート
印刷プレビュー

反応式

HRID 2226975 の反応式
[C:1]([CH2:5][CH2:6][Si:7]([Cl:10])(Cl)[Cl:8])([F:4])([F:3])[F:2].[C:11]([CH2:15][CH2:16][SiH](Cl)Cl)([F:14])([F:13])[F:12]>[H+].[H+].Cl[Pt-2](Cl)(Cl)(Cl)(Cl)Cl>[Si:7]([CH2:6][CH2:5][C:1]([F:4])([F:3])[F:2])([CH2:16][CH2:15][C:11]([F:14])([F:13])[F:12])([Cl:10])[Cl:8]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 689633,3,3-TrifluoropropyltrichlorosilaneHCID 57354963HCID 57354963、化合物2 回

生成物 1

HCID 69583Silane, dichlorobis[3,3,3-trifluoropropyl]-

試薬・触媒・溶媒 1

HCID 61859Chloroplatinic acid触媒

反応条件

温度
50 °C

実験手順

2 moles CF3CH2CH2SiCl3, 3.5 moles Me2SiHCl, and 2.6 moles tetra(n-butyl)ammonium chloride were introduced into a flask and heated under reflux for 3 days with stirring. A mixture of chlorosilanes was then recovered by distillation in vacuo. According to analysis by gas chromatography, the main components of the reaction product were CF3CH2CH2SiCl3, CF3CH2CH2SiHCl2, Me2SiHCl, and Me2SiCl2. The CF3CH2CH2SiCl3 and CF3CH2CH2SiHCl2 fraction was isolated by distillation in vacuo. The CF3CH2CH2SiCl3 and CF3CH2CH2SiHCl2 mixture was placed in a flask, 5 g isopropanolic chloroplatinic acid solution (concentration=10%) was added, and, while stirring and heating to 50° C., CF3CH=CH2 gas was then continuously injected through a glass tube inserted into the liquid. Its addition was halted when the peak for CF3CH2CH2SiHCl2 had disappeared in gas chromoatographic analysis. (CF3CH2CH2)2SiCl2 (bp=128° C./20 mmHg) was then isolated by distillation in vacuo.

後処理

  1. customCF3CH=CH2 gas was then continuously injected through a glass tube
  2. additionIts addition

出典と根拠

ORDレコード
ord-c8dbc4f514bc47d0b7cc77167022458e
出典データセット
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05350824

反応ノート

読み込み中…

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