Process for the production of substituted acetonitriles
AssigneeDegussa AG
InventorsPeter Schalke, Axel Kleemann
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Abstract
The known synthesis for the production of aromatic substituted acetonitriles by reaction of aromatic substances with cyanogen chloride in the gas phase is improved by feeding the starting materials in gaseous form and separated from each other into the reactor. The process can be used to synthesize in general aromatic and especially hetero-aromatic substituted acetonitrile.
Claims31
A process for the production of an aromatic or heteroaromatic substituted acetonitrile of the formula ##STR2## where R.sub.1 is hydrogen, phenyl, thienyl, pyridyl, quinolyl or isoquinolyl and R.sub.2 is thienyl, pyridyl, quinolyl or isoquinolyl or R.sub.2 is a substituted thienyl, pyridyl, quinolyl or isoquinolyl group having at least one substituent wherein the substituent is lower alkyl, halogen, hydroxy, cyano, phenoxy or methoxy and n is 0 or 1 comprising reacting a substituted methane of the formula R.sub.1 --CH.sub.2 --R.sub.2, toluene or hydroxytoluene with cyanogen chloride in the gas phase by feeding the substituted methane and cyanogen chloride separately from each other and in gaseous form into the reactor at a temperature close to the reaction temperature and carrying out the reaction at a temperature between 550.degree. and 850.degree. C., cooling the reaction mixture immediately after leaving the reactor to a temperature below 100.degree. C. and treating the reaction mixture with an aqueous base.
Dependencies are inferred from the claim text.