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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromopent-2-yne | HCID 85399 | — |
| Reactant | (R)-Quinuclidin-3-yl 2-hydroxy-2,2-di(thiophen-2-yl)acetate | HCID 44232927 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (R)-3-(2-Hydroxy-2,2-di-thiophen-2-yl-acetoxy)-1-pent-2-ynyl-1-azonia-bicyclo[2.2.2]octane bromide | HCID 67496709 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08168654B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-98009d84318443ad83673bcd97d264e9 |
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| Source note | uspto-grants-2012_05 |
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