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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078376Generated: November 1, 2026

Hydrochloric Acid → 7-Amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptane

https://huagongshe.com/reaction/2078376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant5-Benzyl-7-t-butoxycarbonylamino-4-oxo-7-methyl-5-azaspiro[2.4]heptaneHCID 57758653—
SolventTolueneHCID 1140—
Product7-Amino-5-benzyl-4-oxo-7-methyl-5-azaspiro[2.4]heptaneHCID 5758730690.2%

Reaction Steps

5-Benzyl-7-t-butoxycarbonylamino-4-oxo-7-methyl-5-azaspiro[2.4]heptane (43.63 g) was dissolved in toluene, and the solution was stirred under ice-cooling. 37% Concentrated hydrochloric acid (100 mL) was added dropwise thereto, followed by stirring. After 0.5 hours, water was added to the reaction mixture. The mixture was stirred and left to stand so as to separate the aqueous layer from the organic layer. Sodium hydroxide (54 g) was added to and dissolved in the separated aqueous layer so as to alkalify the layer. The aqueous layer was extracted several times with toluene repeatedly. All the toluene layers were combined and washed with saturated brine. The washed toluene layer was dried with sodium sulfate, followed by filtration. The filtrate was concentrated under reduced pressure, to thereby yield the title product (21.29 g, yield: 90.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928232B2
Source datasetuspto-grants-2011_04
ORD IDord-ad9accac260647338927e0da08e5e6eb
Source noteuspto-grants-2011_04