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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637877Generated: October 30, 2026

Acetic Acid → Oxcarbazepine

https://huagongshe.com/reaction/637877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantBoron trifluorideHCID 6356—
Reactant10-Nitro-5H-dibenz(b,f)azepine-5-carbonitrileHCID 22467891—
CatalystIronHCID 23925—
ProductOxcarbazepineHCID 34312—

Reaction Steps

50 ml of a solution of 15% by weight of BF3 in acetic acid (=0.11 mole) are added to a suspension of 26.3 g (0.1 mole) of 5-cyano-10-nitro-5H-dibenz[b,f]azepine in 100 ml of acetic acid at room temperature. In the course of this the temperature rises slowly to 34° with complete dissolution of the starting material. 30 ml of water are added at 30° in the course of 5 minutes, resulting in a further increase in temperature to 37°. At this temperature 40 g of iron powder are added in portions over a period of 20 minutes, the temperature being maintained at 65°-70° by occasional cooling. After the exothermic reaction has subsided, stirring is continued for a further 15 minutes and then inorganic material is filtered off and washed three times with a little acetic acid. The total filtrate is added dropwise, while stirring well, to 11/2 l of water and, after stirring for 2 hours, the resulting precipitate is filtered off and washed neutral with water. After drying in vacuo at 60°, 5-carbamoyl-10-oxo-10,11-dihydro-5H-dibenz[b,f]azepine is obtained, which according to the IR spectrum is identical to authentic material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559174
Source datasetuspto-grants-1985_12
ORD IDord-7cd6b0bbbb3d49eb96ba3e6b2b854ec0
Source noteuspto-grants-1985_12