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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Disilane → 1,2-Diethoxy-1,1,2,2-tetramethyldisilane

HRID 1781451
ノート
印刷プレビュー

反応式

HRID 1781451 の反応式
[CH3:1][Li].[SiH3][SiH3].[CH3:5][Si:6]([CH3:18])([O:15][CH2:16][CH3:17])[Si:7]([CH3:14])([O:11][CH2:12][CH3:13])OCC>>[CH3:18][Si:6]([CH3:5])([O:15][CH2:16][CH3:17])[Si:7]([CH3:1])([CH3:14])[O:11][CH2:12][CH3:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 74123DisilaneHCID 141459601,1,2-Triethoxy-1,2,2-trimethyldisilaneHCID 178418348HCID 178418348、化合物2 回

生成物 1

HCID 112757741,2-Diethoxy-1,1,2,2-tetramethyldisilane

実験手順

In the same manner as in Example 1, change of the average molecular weight of the resulting polysilanes was examined by changing the amount of methyl lithium to be used as a reaction starting compound. The results including those of Example 1 and the yields and properties of the products are shown in Table 1. In Example 4, after the disilane compound and methyl lithium were reacted, the reaction mixture was applied to gas chromatography before heating to confirm that 1,1,2-trimethyl-1,2,2-triethoxydisilane and 1,1,2,2-tetramethyl-1,2-diethoxydisilane were produced. From the reaction mixture of Example 4, no solid was obtained by reprecipitation so that low boiling point compounds were removed under conditions of 180° C. and 1 Torr to give a final product.

後処理

  1. customthe yields
  2. temperaturebefore heating

出典と根拠

ORDレコード
ord-2d606d6d3667474d86be1b3b1f0f8478
出典データセット
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05633312

反応ノート

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