HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → Sec-butoxy cyclopentyl dimethoxysilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | (+-)-2-Butanol | HCID 6568 | — |
| Reactant | Cyclopentyltrimethoxysilane | HCID 9855701 | — |
| Catalyst | Sodium Methoxide | HCID 10942334 | — |
| Product | Sec-butoxy cyclopentyl dimethoxysilane | HCID 18925834 | 84.3% |
Reaction Steps
In a 100 ml three-neck flask provided with a magnetic stirrer were charged 10.3 g (0.0542 mole) of cyclopentyl trimethoxysilane, 40.3 g (0.543 mole) of sec-butyl alcohol and 33.7 mg (0.625 m mole) of sodium methoxide, which were then reacted with each other at room temperature for 2 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 10.6 g (0.0457 mole) of sec-butoxy cyclopentyl dimethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. FIGS. 1 and 2 are charts of 1H-NMR and IR, respectively. The yield was 84%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05248803 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-10db705dac8b406da8c9efae3471dda0 |
| Source note | uspto-grants-1993_09 |