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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533804Generated: October 28, 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/533804

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 numberUS08853404B2
Source datasetuspto-grants-2014_10
ORD IDord-38c45784d6454158b87174f507390329
Source noteuspto-grants-2014_10