Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | HCID 20613751 | HCID 20613751 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 20613752 | HCID 20613752 | — |
Reaction Steps
Formic acid (98%, 2.9 mL) and acetic anhydride (1.0 mL) were combined under an inert atmosphere while cooling with a cold water bath. (R)-N-(1-Azabicyclo[2.2.2]oct-3-yl)(E-3-(2-aminophenyl)propenamide) (0.16 g, 0.00059 moles) was added and the reaction was stirred for three days at room temperature. The solution was poured into saturated sodium carbonate and more solid carbonate was added until the solution was basic. The aqueous layer was extracted four times with chloroform. The organic extracts were combined, dried (MgSO4), and concentrated in vacuo. The product was transferred using chloroform and this was stripped and chased with two portions of ether. The white solid was dried at room temperature with high vacuum, giving 64 mg; MS (ES+) 300 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06683090B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-6631348781b24a70bcf6cbbf2b4a56bd |
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| Source note | uspto-grants-2004_01 |
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