http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0792254-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2aea911a292375f04092023a894cd417
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 1995-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1592298f5a3e098c93b6bd0292ff732f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc9a3eb290eab1aaff1420c7310e7fcb
publicationDate 1997-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0792254-A1
titleOfInvention Synthesis of bis(2,2-dinitropropyl)acetal (bdnpa)
abstract A nonsolvent process of synthesizing bis(2,2-dinitropropyl)acetal (BDNPA) is disclosed. In the process, 2,2-dinitropropanol (DNPOH) is reacted at low temperature with an acetaldehyde source in the presence of an acid catalyst, such as a Lewis acid catalyst or protic acid catalyst. To inhibit byproduct formation, the reaction temperature is maintained from about -30 °C to 30 °C. Upon completion of the reaction, the reaction solution is quenched with water and washed with an aqueous hydroxide solution. The hydroxide concentration should be sufficient to neutralize any acid formed during the quenching step and to solubilize unreacted 2,2-dinitropropanol as well as other aqueous soluble by products in the reaction solution. The BDNPA product is extracted with methyl tert-butyl ether (MTBE) or equivalent solvent. The organic solvent is evaporated to yield usable BDNPA product. The resulting yield is at least 50 % based on the starting quantity of 2,2-dinitropropanol.
priorityDate 1994-11-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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