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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10344Generated: October 28, 2026

Ethyl 5-benzyl-5-azaspiro[2.4]heptane-7-carboxylate → HCID 21978858, compound

https://huagongshe.com/reaction/10344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-benzyl-5-azaspiro[2.4]heptane-7-carboxylateHCID 21979521—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
ProductHCID 21978858HCID 2197885854.6%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution (−78° C.) of 5-benzyl-5-azaspiro[2.4]heptane-7-carboxylic acid ethyl ester (Example A1a, 8.15 g, 31.4 mmol) in diethyl ether (200 mL) under a nitrogen atmosphere is treated with methyllithium (1.4 M in diethyl ether, 22.4 mL, 31.4 mmol) over a period of 10 minutes. After 1 hour, reaction mixture is warmed to −10° C. and quenched with saturated aqueous ammonium chloride. The mixture is poured into a separatory funnel and the organic layer is washed with saturated aqueous ammonium chloride, water, and brine. The organic layer is then dried with MgSO4, filtered, and the filtrate concentrated. The resulting residue is purified via flash column chromatography (1% triethylamine/7% isopropanol/92% CH2Cl2) to afford the title compound (3.93 g). MS CI: m/z 230 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094780B1
Source datasetuspto-grants-2006_08
ORD IDord-1a920b8fb152448dab5ca2e70769c5b9
Source noteuspto-grants-2006_08