Acetylene → 1,1,1,4,4,4-Hexachloro-1,4-disilabutane

HRID 2295164

反応式

HRID 2295164 の反応式
[CH:1]#[CH:2].[SiH:3]([Cl:6])([Cl:5])[Cl:4]>>[Si:3]([CH2:1][CH2:2][Si:3]([Cl:6])([Cl:5])[Cl:4])([Cl:6])([Cl:5])[Cl:4]

参加物

3

反応物 2

HCID 6326AcetyleneHCID 24811Trichlorosilane

生成物 1

HCID 756311,1,1,4,4,4-Hexachloro-1,4-disilabutane

実験手順

An example is the reaction of acetylene with HSiCl3 to give Cl3 SiCH2CH2SiCl3 in the first step of the process. An intermediate produced is CH2 =CHSiCl3, which can be used as starting material in place of acetylene and, when reacted with HSiCl3, leads to the same end product of the first step of the process, Cl3SiCH2CH2SiCl3.

出典と根拠

ORDレコード
ord-5e754ed0131e43f193ce4c37b2265979
出典データセット
uspto-grants-1997_11
特許番号
US05691435

関連ノート

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