Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920554Generated: October 28, 2026

1-Bromopent-2-yne → (R)-3-(2-Hydroxy-2,2-di-thiophen-2-yl-acetoxy)-1-pent-2-ynyl-1-azonia-bicyclo[2.2.2]octane bromide

https://huagongshe.com/reaction/1920554

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromopent-2-yneHCID 85399—
Reactant(R)-Quinuclidin-3-yl 2-hydroxy-2,2-di(thiophen-2-yl)acetateHCID 44232927—
SolventChloroformHCID 6212—
Product(R)-3-(2-Hydroxy-2,2-di-thiophen-2-yl-acetoxy)-1-pent-2-ynyl-1-azonia-bicyclo[2.2.2]octane bromideHCID 67496709—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 1-bromo-2-pentyne (0.51 g, 3.44 mmol) in chloroform (2 ml) is treated with polymer supported TEA resin. After a few minutes this solution is added to a solution of hydroxy-di-thiophen-2-yl-acetic acid (R)-(1-aza-bicyclo-[2.2.2]oct-3-yl) ester (Example 70(ii)) (1.0 g, 2.87 mmol) in chloroform (2 ml). The resulting mixture is heated to 50° C. for 18 h and the mixture allowed to cool to room temperature. A white solid is isolated by filtration, washed with chloroform and dried. Recrystallisation from chloroform-acetonitrile, washing the resultant solid with cold acetonitrile, and drying under vacuum gives (R)-3-(2-Hydroxy-2,2-di-thiophen-2-yl-acetoxy)-1-pent-2-ynyl-1-azonia-bicyclo[2.2.2]octane bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168654B2
Source datasetuspto-grants-2012_05
ORD IDord-98009d84318443ad83673bcd97d264e9
Source noteuspto-grants-2012_05