http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4038284-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-04
filingDate 1976-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1977-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8891b243ff0883200f53e3b989e5155
publicationDate 1977-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4038284-A
titleOfInvention N-acylation of oxazolidines
abstract N-substituted oxazolidines having the formula ##STR1## in which R is C 1 -C 10 haloalkyl, C 1 -C 10 alkyl or lower alkylthio; and R 1 and R 2 are independently hydrogen, C 1 -C 12 alkyl, lower alkoxyalkyl or lower alkylol; and R 3 , R 4 , R 5 and R 6 are independently hydrogen, lower alkyl, lower alkoxyalkyl or lower alkylol are prepared by reacting an oxazolidine with an acid chloride or analogous compound in the presence of a hydrogen chloride acceptor and water. The process is characterized by minimization of by-product formation. n In a preferred embodiment, the oxazolidine is prepared by reaction of an alkanolamine with an aldehyde or ketone and the water of reaction is retained in the system.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0648768-A1
priorityDate 1975-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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