HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389248Generated: October 31, 2026
Water → 7-Amino-5-benzyl-7-methyl-5-azaspiro[2.4]heptane
https://huagongshe.com/reaction/389248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 7-Amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptane | HCID 57587306 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Amino-5-benzyl-7-methyl-5-azaspiro[2.4]heptane | HCID 24962312 | 98.6% |
Reaction Steps
7-Amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptane (27 g) was dissolved in anhydrous tetrahydrofuran (265 mL) in an argon atmosphere, and the solution was cooled with ice. Lithium aluminum hydride (13.3 g) was added thereto, and the mixture was returned to room temperature. After disappearance of the starting materials had been confirmed, the reaction mixture was cooled with ice. Water (200 mL) and 28% aqueous sodium hydroxide solution (70 mL) were added to cooled mixture, followed by stirring. Toluene was added to the mixture for extraction to separate the organic layer, and the organic layer was washed with saturated brine, followed by drying with sodium sulfate. The desiccant was removed through filtration, and the filtrate was concentrated under reduced pressure, to thereby yield the title product (24.7 g, yield: 98.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378119B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-34f45a26566e4bf59024b981fad880cd |
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| Source note | uspto-grants-2013_02 |
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