化工社化工社 化学情報印刷レポート · 研究参考用
Ammonia → 3-Aminopentanenitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Valeronitrile | HCID 8061 | — |
| 反応物 | 2-Methyl-3-butenenitrile | HCID 27909 | — |
| 反応物 | 2-Methyl-2-butenenitrile | HCID 29935 | — |
| 反応物 | 2-Pentenenitrile, (Z)- | HCID 6433944 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | 3-Aminopentanenitrile | HCID 93451 | — |
| 生成物 | 2-Pentenenitrile, (Z)- | HCID 6433944 | — |
反応手順
A mixture of approximately 70 weight percent cis-2-pentenenitrile, 14 weight percent 2-methyl-2-butenenitrile, 4 weight percent 2-methyl-3-butenenitrile, with cyclohexane, benzene, and valeronitrile making up the balance, was reacted with 29 weight percent aqueous ammonia (at 15 percent molar excess relative to cis-2-pentenenitrile) in a stirred batch reactor at about 90° to 100° C., at an autogeneous pressure of about 60 to 118 psig, for approximately ten hours Vacuum distillation of the crude reaction mixture to remove low boiling impurities and water resulted in 91% selectivity to 3-aminopentanenitrile at 97% conversion of the starting cis-2-pentenenitrile
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07973174B2 |
| 出典データセット | uspto-grants-2011_07 |
| ORD ID | ord-1cf7106d406649d68962d86d47430545 |
| 出典メモ | uspto-grants-2011_07 |