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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_73ee0bacab5a7576a6a3244747f6ea99
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filingDate 1934-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1935-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-436805-A
titleOfInvention Manufacture of naphthylamine derivatives
abstract 1-Hydroxyalkylamino-5-naphthols and (or) 1 : 5-di(hydroxyalkylamino)naphthalenes are prepared by treating 1 : 5-dihydroxynaphthalene with a primary hydroxyalkyl amine sulphite in an aqueous medium or with a primary hydroxyalkyl amine in the presence of an aqueous solution of a bisulphite. When a 1-hydroxyalkylamino-5-naphthol is the product desired, the corresponding 1 : 5-di(hydroxyalkylamino)naphthalene may be added to the reaction mixture, to restrain its formation in the reaction. The reaction may be effected under reflux or at 110--115 DEG C. under pressure. In the examples, (1) 1 : 5-dihydroxynaphthalene, ethanolamine, and aqueous sodium bisulphite are heated together and the product is diluted, made strongly alkaline, boiled and cooled, whereupon 1 : 5-di(hydroxyethylamino)-naphthalene separates; the filtrate is acidified to precipitate unchanged 1 : 5-dihydroxynaphthalene, and the filtrate from this is made feebly alkaline to precipitate 1-hydroxyethylamino-5-naphthol; ethanolamine sulphite may be used in place of ethanolamine and sodium bisulphite; (2) 1 : 5-dihydroxynaphthalene, ethanolamine, and aqueous sodium bisulphite are heated together with the addition of 1 : 5-di-(hydroxyethylamino)naphthalene, and the product is worked up as in example 1. Specification 410,843 is referred to.
priorityDate 1934-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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