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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910495Generated: November 1, 2026

2-(Chloroacetyl)thiophene → HCID 86672932, compound

https://huagongshe.com/reaction/1910495

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Chloroacetyl)thiopheneHCID 2757925—
ReactantHCID 70938644HCID 70938644—
SolventEthyl AcetateHCID 8857—
ProductHCID 86672932HCID 8667293269.1%

Reaction Steps

To a solution of (2-chlorophenyl)(4-chlorophenyl)methyl(R)-quinuclidin-3-ylcarbamate (95.0 mg, 0.23 mmol) in ethyl acetate (3 ml), 2-chloro-1-(thiophen-2-yl)ethanone (37.6 mg, 0.23 mmol) was added, and the mixture was stirred at room temperature overnight. The solvent was removed under vacuum, and the residue was taken up in diethyl ether and filtered. The product was purified by flash chromatography (DCM/MeOH=95/5) to obtain (3R)-3-(((2-chlorophenyl)(4-chlorophenyl)methoxy)carbonylamino)-1-(2-oxo-2-(thiophen-2-yl)ethyl)-1-azoniabicyclo[2.2.2]octane chloride (45.0 mg, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604015B2
Source datasetuspto-grants-2013_12
ORD IDord-5e7f92806bc941c7a4cbd88cc314426e
Source noteuspto-grants-2013_12