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HRID 273327作成日:2026年10月27日

Bromoacetone → 7-Methoxy-2-methylindolizine

https://huagongshe.com/reaction/273327

反応式

関与物質

役割名称HCID仕込み量
反応物BromoacetoneHCID 11715—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物4-Methoxy-2-methylpyridineHCID 4737758—
溶媒BenzeneHCID 241—
生成物7-Methoxy-2-methylindolizineHCID 5295161831%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456289B2
出典データセットuspto-grants-2008_11
ORD IDord-6df95fb68b7c47248a73d1d03ad07ace
出典メモuspto-grants-2008_11