HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1,4-Dichloro-2-(trimethoxy)silyl-2-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trichloro(1,4-dichlorobut-2-en-2-yl)silane | HCID 53421800 | — |
| Product | 1,4-Dichloro-2-(trimethoxy)silyl-2-butene | HCID 54410263 | 80% |
Reaction Steps
A solution of 14.2 g (55 mmol) of 1,4-dichloro-2-(trichloro)silyl-2-butene [VI]in 7 ml of THF was cooled to -10° C., to which was slowly added dropwise a mixed solution of 10 ml of CH3OH (55×3×1.5 mmol) and 34.5 ml of (C2H5)3N (55 x 3 x 1.5 mmol). Then, it was stirred at room temperature for one hour and 30 ml of dry ether were added. After filtering out the (C2H5)3N·HCl and removing the solvent through distillation under a reduced pressure, 10.8 g of 1,4-dichloro-2-(trimethoxy)silyl-2-butene [VII](yield: 80 %, bp: 88°-90° C./1-2 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837339 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-fd685ebaf13d47f39f6444a89b19df03 |
| Source note | uspto-grants-1989_06 |