Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619531Generated: November 3, 2026

Phenacyl bromide → HCID 86665840, compound

https://huagongshe.com/reaction/1619531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 67607323HCID 67607323—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductDiisopropyl EtherHCID 7914—
ProductHCID 86665840HCID 8666584099.8%

Reaction Steps

2-Bromo-1-phenylethanone (34.7 mg, 0.17 mmol) is added to a solution of (R)-quinuclidin-3-yl 2-(tert-butoxycarbonylamino)-2-(4-fluorophenyl)-acetate (C50) (60.0 mg, 0.16 mmol) in EtOAc (2 ml) and acetonitrile (2 ml). The reaction was stirred at RT for 15 hours, and then the solvent was evaporated. The resulting residue was triturated with i-Pr2O/EtOAc (10/1) and then i-Pr2O to obtain (3R)-3-(2-(tert-butoxycarbonyl-amino)-2-(4-fluorophenyl)acetoxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo-[2.2.2]octane bromide (46.1 mg; 50% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772314B2
Source datasetuspto-grants-2014_07
ORD IDord-59d3acee70ee42c28a1b2a78dd3a68f0
Source noteuspto-grants-2014_07