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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d66aced64b418a4f422589fa7eee73a2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C323-00
filingDate 1938-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1940-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-518775-A
titleOfInvention An improved manufacture of phenol sulphides
abstract 518,775. Alkyl phenol sulphides. STANDARD OIL DEVELOPMENT CO. Sept. 1, 1938, No. 25600. Convention date, Dec. 4, 1937. [Class 2 (iii)] Alkyl phenol sulphides are prepared by heating an alkyl phenol with sulphur and an inorganic alkaline compound of an alkali metal, e.g., sodium carbonate, hydroxide or sulphide; in the presence of a non-aqueous inert solvent until the evolution of hydrogen sulphide ceases, and liberating the free alkyl phenol sulphide from the resultant solution of its alkali metal salt. The phenols may contain more than one alkyl group and more than one hydroxyl group. They preferably contain up to 8 carbon atoms in the alkyl group. Phenols mentioned are cresol, ethyl, propyl butyl, tert. butyl, amyl, tert. amyl, heptyl, hexyl, iso-octyl and di-iso-butyl phenols. Suitable inert solvents are those boiling above 130‹C., e.g., xylene, saturated hydrocarbons or hydrogenated compounds, glycermic or ethylene glycol. Molecular quantities of the various components are preferably used to obtain a mono- or poly-sulphide. The reaction is performed at 100-200‹C. and preferably at atmospheric temperature and with agitation. The sulphide may be purified by percolation, through clay or sodium carbonate. In an example para-tertiary butyl phenol, flowers of sulphur, and anhydrous sodium carbonate were heated in glycerol. After acidifications the butyl phenol sulphide was extracted with ether, dried with sodium sulphate and purified by distillation.
priorityDate 1937-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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