HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dichloro-2-butyne → Trichloro(1,4-dichlorobut-2-en-2-yl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dichloro-2-butyne | HCID 13182 | — |
| Reactant | Trichlorosilane | HCID 24811 | — |
| Reactant | 2-Trichlorosilyl-1,3-butadiene | HCID 13330891 | — |
| Reactant | Silyl-1,3-butadiene | HCID 123285678 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Product | Trichloro(1,4-dichlorobut-2-en-2-yl)silane | HCID 53421800 | — |
Reaction Steps
For instance, 2-trichlorosilyl-1,3-butadiene [II-d]and 2-triloweralkoxy silyl-1,3-butadiene [II-a]can be synthesized by reacting 1,4-dichloro-2-butyne [IV]and trichlorosilane [V]in the presence of a platinum type catalyst to obtain 1,4-dichloro-2-(trichloro)silyl-2-butene [VI]is then reacted with Zn in a tetrahydrofuran solvent to prepare 2-(trichloro)silyl-1,3-butadiene[II-d], and further reacting the 2-(trichloro)silyl-1,3-butadiene II-d with a lower alcohol in the presence of a base, such as triethylamine, as shown by the following Formula (C): ##STR14##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837339 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-a9d8a9153da147a882b0dcc26bb4a93d |
| Source note | uspto-grants-1989_06 |