Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | Diethyl acetonedicarboxylate | HCID 66045 | — |
| Reactant | 4,4-Diethoxybutylamine | HCID 80672 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 69592000 | HCID 69592000 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Indolizin-7-ol | HCID 22180983 | 60.7% |
Reaction Steps
To a suspension of lithium aluminum hydride (2.30 g) in tetrahydrofuran (50 ml) was added dropwise indolizin-7-one (2.80 g), which was prepared from 4,4-diethoxybutylamine and diethyl 1,3-acetonedicarboxylate according to the method described in Heterocycles, 43, 1391 (1996), with stirring under ice-cooling under a nitrogen atmosphere, and the resulting mixture was stirred at the same temperature for 1 hour. After stirring, to the reaction mixture was added sodium sulfate decahydrate, and the resulting mixture was furthermore stirred at room temperature for 1 hour. After removing insoluble materials by filtration, the filtrate was evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of dichloromethane and methanol (4:1) as the eluent to afford the title compound (1.70 g, yield: 59%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030138B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-9a2aeef1ee1b4da0bb01d0592c1642a7 |
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| Source note | uspto-grants-2006_04 |
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