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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-20
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-10
filingDate 1970-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1972-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b69645d88e0d4afc7f87591436b07708
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publicationDate 1972-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3691198-A
titleOfInvention Synthesis of 1-substituted-3-halopyrrolidines
abstract A method of preparing 1-substituted-3-halopyrrolidines, particularly a method of preparing said pyrrolidines by reacting a 1-substituted- Delta 3-pyrroline with a concentrated hydrogen halide aqueous solution at a temperature greater than 100*C. In a preferred embodiment, a supersaturated hydrobromic acid solution is utilized, i.e., one containing about 60 percent hydrogen bromide. The 1-substituted- Delta 3-pyrroline reactant is preferably made by reaction of a cis-1,4-dihalobutene-2 with a primary amine whereupon cyclization takes place. Said 1substituted-3-halopyrrolidines are intermediates useful in making anti-cholinergics and like materials.
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