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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
Reactant7-Amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptaneHCID 57587306—
SolventTolueneHCID 1140—
Product7-Amino-5-benzyl-7-methyl-5-azaspiro[2.4]heptaneHCID 24962312105,006.602%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378119B2
Source datasetuspto-grants-2013_02
ORD IDord-8e9cf16a956447b1966624755e04305c
Source noteuspto-grants-2013_02