化工社化工社 化学情報印刷レポート · 研究参考用
Thionyl Chloride → Methyl 3-(4-pentenoylamino)benzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 4-Pentenoic acid | HCID 61138 | — |
| 反応物 | Benzoic acid, 3-amino-, methyl ester | HCID 78274 | — |
| 反応物 | 4-Pentenoyl chloride | HCID 4228493 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Methyl 3-(4-pentenoylamino)benzoate | HCID 10775994 | 32% |
反応手順
Methyl(3-amino)benzoate (4.5 g, 29.8 mmol) was taken up in DCM (10 ml) and pyridine (1 ml) at 0° C. 4-Pentenoyl chloride (freshly prepared from 4-pentenoic acid (3.0 g, 29.97 mmol) and thionyl chloride (6.6 ml) at r.t. for 1 h, evaporated and azeotroped with DCM) was added dropwise in DCM (3 ml). The mixture was allowed to warm to r.t. and stirred overnight. The mixture was evaporated and partitioned between EtOAc and 1M HCl. The organic portion was washed with 5% KHCO3 and brine, filtered (Whatman® 1PS, phase separator), and evaporated. The residue was chromatographed (eluant 30% EtOAc in hexanes) to provide a colourless oil (2.20 g, 32%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05728829 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-21d973d5e9c342b28599ca4532af6af7 |
| 出典メモ | uspto-grants-1998_03 |