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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B11-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B67-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-24
filingDate 1990-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-05-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5522e5a9238528ca5f49401a3382b5df
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b3ba57a1c190822f5697df74ff7b0fc5
publicationDate 1992-05-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5110952-A
titleOfInvention Method of producing 3-dibutylamino 6-methyl-7-anilinofluoran
abstract A method of producing a high melting point 3-dibutyl amino-6-methyl-7-anilinofluoran characterized by peaks at diffraction angle (2 θ) of 6.9°, 11.0°, 18.5° and 18.9° in X-ray diffractiometry using Cu-K α ray and having a melting point in the range of 179°-186° C., which comprises: condensing 2-(4-dibutylamino-2-hydroxy-benzoyl) benzoic acid with 4-methoxy-2-methyldiphenylamine in the presence of concentrated sulfuric acid to provide a phthalide at a temperature in the range of 0°-50° C., neutralizing the phthalide, and then subjecting the phthalide to ring closure reaction using an alkali in an amount of 0.5-15 mols per mol of the compound used in smaller amounts of 2-(4-dibutylamino-2-hydroxy-benzoyl) benzoic acid and 4-methoxy-2-methyldiphenylamine at a temperature of not less than 50° C. in the presence or absence of an organic solvent.
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priorityDate 1989-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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