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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 5-benzyl-5-azaspiro[2.4]heptane-7-carboxylate | HCID 21979521 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21978858 | HCID 21978858 | 54.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094780B1 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-1a920b8fb152448dab5ca2e70769c5b9 |
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| Source note | uspto-grants-2006_08 |
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