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Methyldichlorosilane → Dichloro(3-phenylpropyl)silane

HRID 2268199
ノート
印刷プレビュー

反応式

HRID 2268199 の反応式
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH3:9][SiH:10]([Cl:12])[Cl:11].C1(NS(=O)(=O)[O-])CCCCC1.[Na+]>[Pt].C1(C)C=CC=CC=1>[CH2:1]([CH2:9][SiH:10]([Cl:12])[Cl:11])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6376Methyldichlorosilane2 回HCID 7501Styrene3 回HCID 23665706Sodium Cyclamate2 回

生成物 1

HCID 71431464Dichloro(3-phenylpropyl)silane収率 70%

試薬・触媒・溶媒 2

HCID 23939Platinum触媒HCID 1140Toluene
溶媒

実験手順

Reaction between styrene and methyldichlorosilane with platinum catalyst in the presence of sodium cyclohexylsulfamate. 427 mg Styrene and 498 mg methyldichlorosilane were introduced into a glass tube, and 38 mg of sodium cyclohexylsulfamate were added. 1 mg Of a toluene solution of a 0-valent platinum complex of divinylsiloxane (0.4 wt % platinum content) was added. The tube was sealed and placed in a 50° C. oil bath where it was heated for 72 hours. After cooling, the tube contents were analyzed by gas chromatography revealing a styrene conversion of 85% and a phenethylmethyldichlorosilane yield of 70%. The ratio between the phenethylmethyldichlorosilane and the (α-methylbenzyl)methyldichlorosilane was 8.7:1.

後処理

  1. customThe tube was sealed
  2. customplaced in a 50° C.
  3. temperaturewas heated for 72 hours
  4. temperatureAfter cooling

出典と根拠

ORDレコード
ord-e0d60dd03ea14e9eb223ccb92a5f57de
出典データセット
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06326506B1

反応ノート

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