http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104710366-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e9854f4ac84f2fce0a2f6f6bdef83b6f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06M13-432
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-40
filingDate 2013-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95dcd3db4532957b72b454ff08bcc5bf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f6fe16d0d8deace82561c2bb651f5dd
publicationDate 2015-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104710366-A
titleOfInvention Improved preparation method of dimethylol dihydroxy ethylene urea
abstract The invention provides a preparation method of dimethylol dihydroxy ethylene urea. The method comprises the following steps: 1, reacting urea with glyoxal in the presence of sulfonic acid and sulfonic acid alkali metal salt at 30-60DEG C for 3-6h to prepare a dihydroxy ethylene urea intermediate; and 2, reacting the dihydroxy ethylene urea intermediate obtained in step 1 with a formaldehyde and optional organic alcohol amine mixture in the presence of dialkali metal hydrogen phosphate and alkali metal dihydrogen phosphate at 40-60DEG C for 2-4h to obtain a target product. The preparation method has the advantages of stable reaction and high conversion rate, and the product has the advantages of high content of active groups, and strong responsivity.
priorityDate 2013-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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