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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404655Generated: October 30, 2026

Phenacyl bromide → HCID 86688914, compound

https://huagongshe.com/reaction/404655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 86688913HCID 86688913—
SolventAcetonitrileHCID 6342—
ProductHCID 86688914HCID 8668891461.9%

Reaction Steps

(R)-quinuclidin-3-yl 2-(3,5-dimethylpiperidin-1-yl)-2-phenylacetate (120 mg, 0.34 mmol) and 2-bromo-1-phenylethanone (73.7 mg, 0.37 mmol) were dissolved in acetonitrile (5 ml) and stirred at room temperature for 16 hours. Acetonitrile was evaporated, the residue was taken up with little EtOAc (2 ml) and then Et2O was added. The white solid that precipitated out was recovered by suction filtration and washed on the filter paper with Et2O. The solid was dried to obtain (3R)-3-(2-(3,5-dimethylpiperidin-1-yl)-2-phenylacetoxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide (115.8 mg, 61.9% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748613B2
Source datasetuspto-grants-2014_06
ORD IDord-82e1b2dacb1e4a92bd56dd825da16b40
Source noteuspto-grants-2014_06