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filingDate 1981-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18f8155bfab4803485ace6fcd0307ca1
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publicationDate 1982-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4341719-A
titleOfInvention Process for the preparation of 1-amino-2-ethoxy-naphthalene-6-sulphonic acid
abstract A process for the preparation of 1-amino-2-ethoxy-naphthalene-6-sulphonic acid from 2-hydroxy-naphthalene-6-sulphonic acid which comprises: n A. contacting 2-hydroxy-naphthalene-6-sulphonic acid with at least an equimolar amount of an alkali metal nitrite in aqueous solution or suspension in the presence of hydrochloric acid, solution or suspension having a pH in the range of 2 to 5 and being at a temperature of 0° to 20° C.; n B. reducing the reaction product of step A in an aqueous suspension by contacting the same with excess iron in the presence of at least an equivalent amount of iron-II ions, relative to the reaction product obtained according to step A, in the presence of a mineral acid at a temperature from 50° to 120° C., and treating the thus-obtained reaction mixture with aqueous alkali metal hydroxide in the presence of iron oxide; n C. contacting the product of step B with excess acetic anhydride in an aqueous solution or suspension at a pH in the range of 3 to 10 at a temperature from 0° to 100° C.; n D. contacting the product of step C with an ethylating agent in the presence of an acid binding agent in an aqueous-organic solvent or diluent in a pH range from 8 to 14 at a temperature from 20° to 150° C.; and n E. deacetylating the product of step D by contacting the same at reflux with an aqueous alkali metal hydroxide.
priorityDate 1980-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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