Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167547Generated: October 31, 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/2167547

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 numberUS09045469B2
Source datasetuspto-grants-2015_06
ORD IDord-ac6b4956f0a24de982b7ab09d22d057e
Source noteuspto-grants-2015_06