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filingDate 1950-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1952-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-682280-A
titleOfInvention Purification of ortho-methoxyphenylacetone
abstract In a method for the purification of o-methoxyphenylacetone containing as impurities one or more aldehydes and/or other ketones and/or one or more other organic compounds which form more readily than o-methoxyphenylacetone an addition complex with a bisulphite, crude o-methoxyphenylacetone is brought into contact with an alkali metal bisulphite, and the o-methoxyphenylacetone is separated in purified form from the complex formed between the bisulphite and the impurities present. The bisulphite may be in the form of finely-divided solid, but is preferably used in aqueous solution. The crude o-methoxy phenylacetone may be dissolved in a water-immiscible organic solvent, e.g. benzene, toluene, chloroform dichlorethane, ether, petroleum ether or ethyl acetate. Examples describe the separation of purified o-methoxyphenylacetone from a mixture of (1) a toluene solution of crude o-methoxyphenylacetone obtained by Experiment 2 of Specification 671,240, and aqueous sodium bisulphite solution; (2) the separated product of (1) and further bisulphite solution; (3) 85.5 per cent o-methoxyphenylacetone and 14.5 per cent o-methoxybenzaldehyde with solid sodium bisulphite; (4) as in (3) but with aqueous sodium bisulphite. The bisulphite addition compound is treated with concentrated hydrochloric acid and the liberated o-methoxybenzaldehyde is recovered; (5) a benzene solution of o-methoxyphenylacetone and o-methoxybenzaldehyde with aqueous sodium bisulphite.
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