HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → Tert-amyloxy cyclopentyl dimethoxysilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | Cyclopentyltrimethoxysilane | HCID 9855701 | — |
| Catalyst | Sodium Methoxide | HCID 10942334 | — |
| Product | Tert-amyloxy cyclopentyl dimethoxysilane | HCID 10988602 | 82% |
Reaction Steps
In a 100 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 10.1 g (0.0531 mole) of cyclopentyl trimethoxysilane, 30.6 g (0.347 mole) of tert-amyl alcohol and 86.4 mg (1.6 m mole) of sodium methoxide, which were then reacted with each other in an oil bath of 105° C. for 4 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 10.7 g (0.0434 mole) of tert-amyloxy cyclopentyl dimethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 82%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05248803 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-44523718c32f4f8db78be90afe1a804e |
| Source note | uspto-grants-1993_09 |