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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434148Generated: October 25, 2026

Chloroacetic Acid → Oxcarbazepine

https://huagongshe.com/reaction/434148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
Reactant10-MethoxyiminostilbeneHCID 78424—
ReactantSodium CyanateHCID 517096—
SolventTolueneHCID 1140—
ProductOxcarbazepineHCID 3431224.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 100 gms of 10-methoxyiminostilbene in 1000 mL of toluene containing 106 gms of monochloro-acetic acid and 73 gms of sodium cyanate were heated to 40° C. under stirring and maintained for 4 hours. After completion of the reaction (monitored by HPLC and/or TLC), the mixture was cooled to room temperature, filtered and washed with 5% sodium carbonate solution followed by water. The toluene layer was then added to 1000 mL of 2N hydrochloric acid, and the mixture was heated to 75-80° C. and maintained for 2 hours under good agitation. It was then cooled to 0-5° C. and maintained for 2 hours, and the product oxcarbazepine was separated by filtration. This was then purified twice in toluene:methanol followed by methanol:dichloromethane solvent mixture to furnish 28 gms of pure oxcarbazepine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670472B2
Source datasetuspto-grants-2003_12
ORD IDord-f354caec36ad47a2a20c079ab1ea1e5d
Source noteuspto-grants-2003_12