HuagongsheHuagongshe Chemistry Print Report · For research reference only
Mandelic Acid → 10-methoxy-5H-dibenz(b,f)azepine-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Mandelic Acid | HCID 1292 | — |
| Reactant | 10-Methoxyiminostilbene | HCID 78424 | — |
| Reactant | Sodium Cyanate | HCID 517096 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 10-methoxy-5H-dibenz(b,f)azepine-5-carboxamide | HCID 120031 | — |
Reaction Steps
A suspension of 10 g of 10-methoxyiminostilbene in 250 ml dichloromethane was treated with 17.5 g of sodium cyanate and 24 g of mandelic acid and was heated to reflux for about 6-8 hrs. The reaction mixture was cooled to room temperature and the reaction mixture was washed with distilled water and aqueous sodium bicarbonate and further the organic layer was distilled off completely. The resulting residue was treated with isopropanol; separated solid was filtered and dried to give 10-methoxy carbamazepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530647B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-58bd4edf32fb443ea85d510b7142241e |
| Source note | uspto-grants-2013_09 |