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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C211-46
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-73
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C-
filingDate 1973-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b41a0c46e4f599f3680cfe1a392387b4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb9e49e1b4e94af9c798e8cbc256e139
publicationDate 1975-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2328757-A1
titleOfInvention Process for the preparation of amines
abstract In the title process amides are reacted with hypohalides in the presence of an excess of an alkaline hydroxide at least equal to 0.2 mole/amide group and cpds. of formula R1R2NK (I) (where R1 is sulphonic, sulphonate or sulphamoyl group; R2 is H, Cl, Br or an aliphatic group and X is H, Cl, or Br; NR1R2 also may be a heterocyclic ring contg. at least one sulphonyl or PO-OR3 group near the M atom and R3 is ' or alkl metal; or R1+R2 is CO-R4-CO and R4 is alkylene, R5 is H, Cl or Br and R6 is an aliphatic group) or a polymn. inhibitorsand opt. a prim. or sec. amine is added at the beginning or during the reaction. Inhibitors may also be catalysts and amines are pref. added after mixing hypohalide with amide. Thus anthranite acid is prepd. from a reaction prod. of phthalic anhydride and ammonia by reaction with naClO (javel water) in the presence of sulphamic acid and NaOH.
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priorityDate 1973-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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