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

HRID 2295164

반응식

[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]

참가 물질

반응물 2

HCID 6326Acetylene

HCID 24811Trichlorosilane

생성물 1

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

실험 절차

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.

출처 및 근거

ORD 기록: ord-5e754ed0131e43f193ce4c37b2265979
출처 데이터셋: uspto-grants-1997_11
DOI: 10.6084/m9.figshare.5104873.v1
특허 번호: US05691435

연결된 노트

불러오는 중…