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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404658Generated: October 29, 2026

2-Chloroacetophenone → HCID 86688917, compound

https://huagongshe.com/reaction/404658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroacetophenoneHCID 10757—
ReactantHCID 86688916HCID 86688916—
SolventEthyl AcetateHCID 8857—
ProductHCID 86688917HCID 8668891778%

Reaction Steps

2-Chloro-1-phenylethanone (31.0 mg, 0.20 mmol) was added to a solution of (R)-quinuclidin-3-yl 2-(4,4-difluoropiperidin-1-yl)-2-phenylacetate (24b) (73 mg, 0.20 mmol) in ethyl acetate (3 ml). The reaction was stirred at room temperature overnight. The solvent was evaporated under reduced pressure and the residue was triturated with Et2O (4 ml). A white precipitate was formed and it was collected by suction filtration and dried under vacuum at 40° C. overnight, to obtain (3R)-3-(2-(4,4-difluoropiperidin-1-yl)-2-phenylacetoxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane chloride (81 mg, 78% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748613B2
Source datasetuspto-grants-2014_06
ORD IDord-abba4528e0db4dde953cfb67e9f46e05
Source noteuspto-grants-2014_06