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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant10-MethoxyiminostilbeneHCID 78424—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantHCID 178418852HCID 178418852—
SolventWaterHCID 962—
Product10-methoxy-5H-dibenz(b,f)azepine-5-carboxamideHCID 12003150.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091339B2
Source datasetuspto-grants-2006_08
ORD IDord-ce0dd8900c0f4904b3ae6c61be0151bc
Source noteuspto-grants-2006_08