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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619576Generated: November 2, 2026

Phenacyl bromide → HCID 86665860, compound

https://huagongshe.com/reaction/1619576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 67606929HCID 67606929—
SolventEthyl AcetateHCID 8857—
ProductHCID 86665860HCID 8666586090.5%

Reaction Steps

To a solution of (S)—((R)-quinuclidin-3-yl) 3-(4-(benzyloxy)phenyl)-2-(tert-butoxycarbonylamino)propanoate (590 mg, 1.23 mmol) in EtOAc (15 ml), was added portionwise 2-bromo-1-phenylethanone (232 mg, 1.17 mmol). The reaction was stirred at RT for 16 hours. The solvent was evaporated, and the residue was triturated with Et2O, filtered and dried under vacuum to obtain (R)-3-((S)-3-(4-(benzyloxy)phenyl)-2-(tert-butoxycarbonylamino)propanoyloxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide (720 mg, 86% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772314B2
Source datasetuspto-grants-2014_07
ORD IDord-e500cfdcb8ac49868cce23af9ae52b36
Source noteuspto-grants-2014_07