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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255075Generated: October 25, 2026

2-Bromo-1-(thiophen-3-yl)ethan-1-one → (R)-3-(2-benzylamino-2-phenyl-acetoxy)-1-(2-oxo-2-thiophen-3-yl-ethyl)-1-azonia-bicyclo[2.2.2]octane bromide

https://huagongshe.com/reaction/1255075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(thiophen-3-yl)ethan-1-oneHCID 2776379—
Reactant(R)-quinuclidin-3-yl 2-(benzylamino)-2-phenylacetateHCID 46840418—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(R)-3-(2-benzylamino-2-phenyl-acetoxy)-1-(2-oxo-2-thiophen-3-yl-ethyl)-1-azonia-bicyclo[2.2.2]octane bromideHCID 8664322914.6%

Reaction Steps

To a solution of (R)-quinuclidin-3-yl 2-(benzylamino)-2-phenylacetate (C80) (116 mg, 0.33 mmol) in ethyl acetate (3.31 mL) and acetonitrile (3.31 mL), is added 2-bromo-1-(thiophen-3-yl)ethanone (66.5 mg, 0.32 mmol). The mixture is stirred at RT overnight. The insoluble precipitate is filtered on a buckner funnel and washed with acetonitrile. The clear solution is evaporated and purified by flash chromatography (DCM/EtOH=9/1) to obtain the title compound as a white solid (26 mg, 14% yield, bromide salt, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455646B2
Source datasetuspto-grants-2013_06
ORD IDord-1adc87dcbb8c429ba558afb2fea1ecfc
Source noteuspto-grants-2013_06