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filingDate 1998-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c818b55e34ebcb8a14ec5c68d66723e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed5bcd8d31130c42a82aca3ee0c031f9
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publicationDate 1998-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H10310563-A
titleOfInvention Method for producing chloroketone using oxazoline
abstract PROBLEM TO BE SOLVED: To provide a novel and inexpensive method for continuously producing α-chloroketone using a substituted alkynylamide. (I) cyclizing an alkynylamide to form 5- Forming methylene oxazoline; (Ii) chlorinating 5-methyleneoxazoline with trichloroisocyanuric acid to produce a chlorinated oxazoline intermediate; (Iii) hydrolyzing the chlorinated oxazoline intermediate with an aqueous acid to produce the desired monochloroketone; (Z is alkyl or substituted alkyl, aryl or substituted aryl, heteroaryl or substituted heteroaryl, or phenylene; R is a hydrogen atom or alkyl; R 1 and R 2 are each independently alkyl or Are substituted alkyl groups, or together with the carbon atom to which they are attached, form a cyclic structure)
priorityDate 1997-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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