HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 15219058, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Cyclopentyl(triethoxy)silane | HCID 16217491 | — |
| Product | HCID 15219058 | HCID 15219058 | 64.2% |
Reaction Steps
In a 500 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 29.3 g (0.129 mole) of cyclopentyl triethoxysilane, 165.9 g (2.24 mole) of tert-butyl alcohol and 2.06 g (30.3 m mole) of sodium ethoxide, which were then reacted with each other in an oil bath of 85° C. for 24 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 21.6 g (0.0828 mole) of tert-butoxy cyclopentyl diethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 64%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05359114 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-86c2e2d6d93745adab12d89beb7bc775 |
| Source note | uspto-grants-1994_10 |