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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619547Generated: November 2, 2026

Phenacyl bromide → HCID 86665848, compound

https://huagongshe.com/reaction/1619547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 67607656HCID 67607656—
SolventDichloromethaneHCID 6344—
ProductHCID 86665848HCID 8666584854.2%

Reaction Steps

(R)-quinuclidin-3-yl 2-(4-methoxyphenylsulfonamido)-2-phenylacetate hydrochloride (C68) (96 mg, 0.22 mmol) was dissolved in DCM and washed with 1M K2CO3. The organic phase was dried over Na2SO4, filtered and evaporated. The resulting solid was dissolved in EtOAc (2 ml) and 2-bromo-1-phenylethanone (49.2 mg, 0.25 mmol) was added. The reaction was stirred at RT for 3 hours, and then it was washed with aq. K2CO3, dried over Na2SO4, filtered and evaporated to obtain (3R)-3-(2-(4-methoxyphenylsulfonamido)-2-phenylacetoxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide (75 mg; 53% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772314B2
Source datasetuspto-grants-2014_07
ORD IDord-6a585da42eac4cceb45cbf7ad968e6e4
Source noteuspto-grants-2014_07