HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9717Generated: October 26, 2026
Acetonitrile → 10-methoxy-5H-dibenz(b,f)azepine-5-carboxamide
https://huagongshe.com/reaction/9717
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 10-Methoxyiminostilbene | HCID 78424 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 178418852 | HCID 178418852 | — |
| Solvent | Water | HCID 962 | — |
| Product | 10-methoxy-5H-dibenz(b,f)azepine-5-carboxamide | HCID 120031 | 50.7% |
Reaction Steps
10-methoxy-5H-dibenz(b,f)azepine (29.9 g, 0.134 mol) was added to 300 ml acetonitrile in a three-neck flask (500 ml) equipped with a mechanical stirring apparatus. The mixture was stirred at room temperature for 15 minutes, and then NaOCN (18 g, 0.277 mol) was added, followed by pyridinium p-toluenesulfonate (75 g, 0.3 mol). The mixture was stirred at room temperature for about 4 hours, at which time TLC indicated that the reaction was complete (disappearance of 10-methoxy-5H-dibenz(b,f)azepine). 30 ml water was added, and the mixture stirred for 15 minutes. The solids were filtered and the filtrate was concentrated under vacuum. The semi-solid residue was triturated with acetone to provide a creamy solid, which was dried at 80° C. to provide 18 g (0.068 mol, 50% yield) of 10-methoxy-5H-dibenz[b,f]azepine-5-carboxamide (10-methoxycarbamazepine).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091339B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ce0dd8900c0f4904b3ae6c61be0151bc |
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| Source note | uspto-grants-2006_08 |
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