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Bromoacetone → 7-Methoxy-2-methylindolizine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Bromoacetone | HCID 11715 | — |
| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 反応物 | 4-Methoxy-2-methylpyridine | HCID 4737758 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 7-Methoxy-2-methylindolizine | HCID 52951618 | 31% |
反応手順
4-Methoxy-2-methylpyridine (0.123 g, 1 mmol) and bromoacetone (0.16 mL, 1 mmol) were heated at 95° C. under N2 for 2 h. 1,8-Diazabicyclo-[5.4.0]-undec-7-ene (0.34 mL, 2.2 mmol) in benzene (10 mL) was added. The mixture was then refluxed under N2 for 1 h, poured into ice water, and then extracted with EtOAc. The combined organic layers were washed with water and dried. After the solvent was removed in vacuo, the residue was purified on a silica gel column eluting with EtOAc:Hexane (1:9) and EtOAc to give 7-methoxy-2-methylindolizine (0.050 g, 31%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07456289B2 |
| 出典データセット | uspto-grants-2008_11 |
| ORD ID | ord-6df95fb68b7c47248a73d1d03ad07ace |
| 出典メモ | uspto-grants-2008_11 |