http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H11158154-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7ef01e33058cf740cf2197991be97af1
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-34
filingDate 1997-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7df2644901447d60261a21944b3ec4f2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c319d5f4545eb575f3efadf7329a0f0e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f471718c6e6071acc738e4e0ee1a838
publicationDate 1999-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H11158154-A
titleOfInvention Method for producing 1,3-dialkyl-2-imidazolidinones
abstract PROBLEM TO BE SOLVED: To provide a direct one-stage reaction from an inexpensive starting material, an alkylene carbonate and a monoalkylamine, to give 1,5. 3-Dialkyl-2-imidazolidinones in high yield, It provides an improved process that has fewer by-products and can be easily implemented in large-scale industrial production. SOLUTION: The alkylene carbonate and the monoalkylamine are heated to 50 ° C or higher in the presence of an alkylamine salt of an alkyl carbamic acid. A method for producing 3-dialkyl-2-imidazolidinones.
priorityDate 1997-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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