HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248402Generated: October 30, 2026
Diethyl Ether → 2-(4-Methylphenyl)indolizine
https://huagongshe.com/reaction/248402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Methylpyridine | HCID 7975 | — |
| Reactant | 2-Bromo-4'-methylacetophenone | HCID 69272 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(4-Methylphenyl)indolizine | HCID 346948 | 74.2% |
Reaction Steps
To a stirred solution of 2-picoline (5.12 g) in acetone (10 ml) was added 2-bromo-4'-methylacetophenone (10.4 g) in one portion and the mixture was heated at 80° C. for one hour. After addition of diethyl ether, the crystalline product was collected and washed with diethyl ether. After drying in air for several hours, this product was suspended in water (100 ml) and a solution of sodium bicarbonate (21 g) in water (100 ml) was added dropwise to the suspension. The mixture was stirred at ambient temperature for 45 minutes and refluxed for half an hour. The mixture was diluted with methylene chloride and washed with aqueous saturated sodium chloride. The organic layer was separated, dried over potassium carbonate and filtered. The solvent was removed in vacuo and the resulting solid was recrystallized from benzene to give 2-(4-methylphenyl)indolizine (7.51 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05210092 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-5c1e705bb6024f20850cf9d81a91c740 |
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| Source note | uspto-grants-1993_05 |
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