化工社化工社 化学情報印刷レポート · 研究参考用
Acetic Acid → 3,7-Diazabicyclo(3.3.1)nonane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | 1-Phenethylamine | HCID 7408 | — |
| 反応物 | 1-Benzyl-4-piperidone | HCID 19220 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3,7-Diazabicyclo(3.3.1)nonane | HCID 192720 | — |
反応手順
A mixture of α-methylbenzylamine (10.7 g, 0.088 mol), paraformaldehyde (21.1 g, 0.703 mol), acetic acid (10.2 mL, 0.179 mol) and 1-benzyl-4-piperidone (16.7 g, 0.088 mol) in MeOH (418 mL) was heated at reflux overnight. Upon cooling to room temperature the solvents were removed in vacuo. Water (700 mL) and KOH pellets (11.7 g, 0.209 mol) were added and the mixture was extracted with 3×150 mL CH2Cl2. The organic layer was dried (K2CO3), filtered and the solvent was removed in vacuo. The yellow residues were triturated with hexane and the combined organic solvents were concentrated to provide bispidine (1) as a crude yellow oil (26.7 g, 90%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07038054B1 |
| 出典データセット | uspto-grants-2006_05 |
| ORD ID | ord-2c85c2b1bd86484192e0d660fb7aef68 |
| 出典メモ | uspto-grants-2006_05 |