Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533839Generated: October 28, 2026

Ethyl 1-azabicyclo(2.2.2)octane-4-carboxylate → HCID 68959827, compound

https://huagongshe.com/reaction/533839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-azabicyclo(2.2.2)octane-4-carboxylateHCID 573424—
ReactantHCID 178418370HCID 178418370—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68959827HCID 6895982786.6%

Reaction Steps

A solution of 4-methylphenylmagnesiumbromide (1.0 M in THF, 3.3 mL, 3.3 mmol) was chilled down to 0° C. under Ar. Ethyl 1-azabicyclo[2.2.2]octane-4-carboxylate (0.1509 g, 0.823 mmol) in THF (4 mL) was slowly added to the reaction mixture at 0° C. over 20 min. The reaction was allowed to warm up to room temperature and then heated at 60° C. for 16 h. The reaction was chilled in an ice bath, quenched with saturated NH4Cl, and concentrated under vacuum. The resulting residue was treated with H2O and extracted with EtOAc. The combined organic layers were dried with MgSO4, filtered, and concentrated under vacuum to yield the desired product (0.2291 g, 86.6%). EI-MS m/z 322(M+H+) Rt (1.57 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853404B2
Source datasetuspto-grants-2014_10
ORD IDord-a53b6b43ba654d2d88ab6fe73ad50068
Source noteuspto-grants-2014_10