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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324693Generated: October 29, 2026

Ammonia → 7-Benzylamino-4-oxo-5-azaspiro[2.4]heptane

https://huagongshe.com/reaction/324693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1-(1-Benzylamino-1-cyanomethyl)-1-ethoxycarbonylcyclopropaneHCID 15391046—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
Product7-Benzylamino-4-oxo-5-azaspiro[2.4]heptaneHCID 15429261—

Reaction Steps

An autoclave was charged with 61.3 mg of 1-(1-benzylamino-1-cyanomethyl)-1-ethoxycarbonylcyclopropane, 0.2 ml of Raney nickel and 2.0 ml of ammonia-saturated ethanol, and the contents were stirred at room temperature for 2 hours in an atmosphere of hydrogen under a pressure of 30 kg/cm2. After completion of the reaction, the catalyst was removed by filtration and the resulting filtrate was concentrated under a reduced pressure to obtain 51.3 mg (quantitative) of the title compound in the form of light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218548B1
Source datasetuspto-grants-2001_04
ORD IDord-1b78b40bb35e4dea8b8e9d3cf0420990
Source noteuspto-grants-2001_04