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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927085Generated: November 3, 2026

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

https://huagongshe.com/reaction/1927085

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 numberUS08183257B2
Source datasetuspto-grants-2012_05
ORD IDord-c290cb80295641d3b33439dbc25b8a2e
Source noteuspto-grants-2012_05