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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782448Generated: October 30, 2026

Ethyl 1-azabicyclo(2.2.2)octane-4-carboxylate → 1-Azabicyclo[2.2.2]oct-4-yl(di-2-thienyl)methanol

https://huagongshe.com/reaction/1782448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-azabicyclo(2.2.2)octane-4-carboxylateHCID 573424—
ReactantHCID 178418439HCID 178418439—
SolventTetrahydrofuranHCID 8028—
Product1-Azabicyclo[2.2.2]oct-4-yl(di-2-thienyl)methanolHCID 6886559959.5%

Reaction Steps

A solution of 2-thienyllithium (1.0M in THF, 9.10 mL, 9.10 mmol) was chilled down to −30° C. under Ar. Ethyl 1-azabicyclo[2.2.2]octane-4-carboxylate (0.4196 g, 2.289 mmol) in THF (8 mL) was slowly added to the reaction mixture over 20 min. The reaction was allowed to warm up to room temperature over 16 h. The reaction was quenched with water and then evaporated to dryness. H2O and DCM were added, causing a light brown solid to crash out. This solid was filtered off to give the title compound (0.4161 g, 59.5%). EI-MS m/z 306(M+H+) Rt (1.35 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498440B2
Source datasetuspto-grants-2009_03
ORD IDord-cfd412060c6344eb95f0afe2468f1c7b
Source noteuspto-grants-2009_03