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Phenothiazine → (3-Aminopropyl)dimethylethoxysilane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phenothiazine | HCID 7108 | — |
| 反応物 | Allylamine | HCID 7853 | — |
| 反応物 | Ethoxydimethylsilane | HCID 61772 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (3-Aminopropyl)dimethylethoxysilane | HCID 87575 | 55% |
反応手順
Into the same reactor as used in Example 1, 54.7 parts of allylamine, 1.0 part of phenothiazine and 0.0005 part as platinum atom of the same platinum complex as in Example 1 were charged, 100 parts of dimethylethoxysilane were added at 50° C. through the dropping funnel over 20 minutes, and the reaction was completed by elevating the temperature to 125° C. over 4 hours. After cooling, 5.5 parts of ethanol were added, and distillation was carried out to give 87.8 parts of γ-aminopropyldimethylethoxysilane boiling at 75° to 77° C./18 Torr. This corresponded to 55% yield based on the theoretical amount.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04649208 |
| 出典データセット | uspto-grants-1987_03 |
| ORD ID | ord-13cdf701d4ff45ea9c39380cdfc8c1f7 |
| 出典メモ | uspto-grants-1987_03 |