HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389249Generated: October 29, 2026
Sodium Hydroxide → 7-Amino-5-benzyl-7-methyl-5-azaspiro[2.4]heptane
https://huagongshe.com/reaction/389249
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Reactant | 7-Amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptane | HCID 57587306 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Amino-5-benzyl-7-methyl-5-azaspiro[2.4]heptane | HCID 24962312 | 105,006.602% |
Reaction Steps
A solution (65% toluene solution) of sodium bis(2-methoxyethoxy)aluminum hydride (1.65 kg, 3.5 eq.) in toluene (870 mL) was added to a solution of 7-amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptane (348 g, 1.51 mmol) in toluene (2.62 L), and the mixture was stirred at an internal temperature of 60° C. for 1 hour. The reaction mixture was cooled with ice. Aqueous sodium hydroxide solution (5N) was added to the cooled mixture, and the aqueous layer was extracted with toluene. The thus-obtained organic layers were combined, and the solvent of the combined organic layer was evaporated under reduced pressure, to thereby yield the title product as brown oil (343 g, purity: 81.3%, yield: 100%).
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-8e9cf16a956447b1966624755e04305c |
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| Source note | uspto-grants-2013_02 |
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