Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzoyl bromide | HCID 12056 | — |
| Reactant | HCID 67496660 | HCID 67496660 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67497150 | HCID 67497150 | — |
Reaction Steps
To a stirred suspension of (R)-1-(2-Amino-ethyl)-3-(2-hydroxy-2,2-diphenyl-acetoxy)-1-azonia-bicyclo[2.2.2]octane bromide hydrobromide [50(H)] (0.28 g, 0.517 mmol) in DCM at 0° C. is added triethylamine (0.216 ml, 1.552 mmol) followed by benzoyl bromide (0.122 ml, 1.03 mmol). The reaction mixture is stirred at 0° C. for 1.5 hours and the solvent was removed in vacuo. Purification of the crude residue by chromatography on C18 silica, eluting with water:acetonitrile affords the title compound.
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-8c75ea5762234258862f27f96a56421e |
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| Source note | uspto-grants-2012_05 |
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