化工社化工社 化学情報印刷レポート · 研究参考用
Hexylamine → 1-[(Benzyloxy)carbonyl]-2-[(hexylamino)carbonyl]pyrrolidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hexylamine | HCID 8102 | — |
| 反応物 | 1-Benzyl 2-(4-nitrophenyl) pyrrolidine-1,2-dicarboxylate | HCID 102970 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-[(Benzyloxy)carbonyl]-2-[(hexylamino)carbonyl]pyrrolidine | HCID 21516712 | — |
反応手順
To a solution of 25.9 g. (0.07 mol.) of N-carbobenzoxy-DL-proline p-nitrophenyl ester in 250 ml. of dry tetrahydrofuran is added 14.1 g. (0.140 mol.) of n-hexylamine in 50 ml. of tetrahydrofuran, and the resulting solution is left overnight at room temperature. The solvent is removed in vacuo, the residue is diluted with ether, and this solution is then washed thoroughly with 1 N aqueous sodium hydroxide, water and then dilute hydrochloric acid. On drying the ether solution and concentrating in vacuo, a pale yellow oil comprising 1-[(benzyloxy)carbonyl]-2-[(hexylamino)carbonyl]pyrrolidine is obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03976660 |
| 出典データセット | uspto-grants-1976_08 |
| ORD ID | ord-568e739eac7d4250803e1e8c44164ee0 |
| 出典メモ | uspto-grants-1976_08 |