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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666964Generated: October 31, 2026

Benzene, (3-bromopropoxy)- → Aclidinium Bromide

https://huagongshe.com/reaction/1666964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
Reactant(R)-Quinuclidin-3-yl 2-hydroxy-2,2-di(thiophen-2-yl)acetateHCID 44232927—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductAclidinium BromideHCID 1151974190%

Reaction Steps

0.6 mmol of 2-hydroxy-2,2-dithien-2-ylacetic acid 1-azabicyclo[2.2.2]oct-3(R)yl ester are suspended in 4 ml of CH3CN and 6 ml of CHCl3. 0.48 ml of 3-phenoxypropyl bromide were added to the resulting suspension and the mixture was stirred for 72 h at room temperature in an inert atmosphere. The solvents were subsequently evaporated to yield (90%) of 3(R)-(2-hydroxy-2,2-dithien-2-ylacetoxy)-1-(3-phenoxypropyl)-1-azoniabicyclo[2.2.2]octane bromide. The product is isolated by filtration at room temperature and the level of 3-phenoxypropyl bromide is determined to be 117 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044205B2
Source datasetuspto-grants-2011_10
ORD IDord-a6fe5cd3973e4a57ac27ed7cd670dca0
Source noteuspto-grants-2011_10