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Cyclopentene → Trichlorocyclopentylsilane

HRID 1091187
ノート
印刷プレビュー

反応式

HRID 1091187 の反応式
[Cl:1][SiH:2]([Cl:4])[Cl:3].[CH:5]1[CH2:9][CH2:8][CH2:7][CH:6]=1>[Pt]>[CH:5]1([Si:2]([Cl:4])([Cl:3])[Cl:1])[CH2:9][CH2:8][CH2:7][CH2:6]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8882Cyclopentene2 回HCID 24811Trichlorosilane2 回HCID 178506046HCID 178506046、化合物

生成物 1

HCID 84533Trichlorocyclopentylsilane収率 91%

試薬・触媒・溶媒 1

HCID 23939Platinum触媒

実験手順

The experiment was conducted in substantially the same manner as in Example 1 by preparing a reaction mixture from 19.5 g (0.144 mole) of trichlorosilane, 9.9 g (0.146 mole) of cyclopentene and 0.14 g of the catalyst I corresponding to 238 ppm by weight as platinum based on the total amount of trichlorosilane and cyclopentene and heating the mixture in a polytetrafluoroethylene-made pressure-resistant vessel at 60° C. for 26 hours under a spontaneously produced pressure of 3 kg/cm2G. About 97% of the starting reactants had been reacted at the end of the reaction time as determined by the gas chromatographic analysis. Treatment of the reaction mixture after the reaction was performed in the same manner as in Example 1 to give cyclopentyl trichlorosilane in a yield of 91% as isolated based on the theoretical value.

後処理

  1. customat 60° C.
  2. customfor 26 hours

出典と根拠

ORDレコード
ord-5fa138351e7a4a3dbe0cff36b6e9e1de
出典データセット
uspto-grants-1992_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05084591

反応ノート

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