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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796204Generated: November 2, 2026

Sodium sulfate decahydrate → Indolizin-7-ol

https://huagongshe.com/reaction/1796204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium sulfate decahydrateHCID 62649—
ReactantDiethyl acetonedicarboxylateHCID 66045—
Reactant4,4-DiethoxybutylamineHCID 80672—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 69592000HCID 69592000—
SolventTetrahydrofuranHCID 8028—
ProductIndolizin-7-olHCID 2218098360.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030138B2
Source datasetuspto-grants-2006_04
ORD IDord-9a2aeef1ee1b4da0bb01d0592c1642a7
Source noteuspto-grants-2006_04