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Chlorotrimethylsilane → Cyclopentyl dimethoxy oxa-3-cyclopentyloxysilane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | 3-Furanol, tetrahydro- | HCID 9960 | — |
| 反応物 | Cyclopentyltrimethoxysilane | HCID 9855701 | — |
| 触媒 | Sodium Methoxide | HCID 10942334 | — |
| 生成物 | Cyclopentyl dimethoxy oxa-3-cyclopentyloxysilane | HCID 19793814 | 54% |
反応手順
In a 100 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 7.7 g (0.0404 mole) of cyclopentyl trimethoxysilane, 35.7 g (0.405 mole) of 3-hydroxy tetrahydrofurane and 53.0 mg (0.98 m mole) of sodium methoxide, which were then reacted with each other in an oil bath of 80° C. for 2 hours under stirring. After cooled, trimethylchlorosilane was added to neutralize the alkali. Then, 5.37 g (0.0218 mole) of cyclopentyl dimethoxy oxa-3-cyclopentyloxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 54%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05248803 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-4f67e89866a749378b2de7b9b7e24fbf |
| 出典メモ | uspto-grants-1993_09 |