http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2550716-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b09f893b262cefd50c5e76c4b85d1c0a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-027
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-023
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-023
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-027
filingDate 1975-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5e536283160b23cf2f0cfd133909367
publicationDate 1977-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2550716-A1
titleOfInvention PROCESS FOR THE PREPARATION OF 2-ALKYLPIPERIDINES
abstract 2-Alkyl piperidines are prepd. by hydrogenation of 2-alkyl pyridines, at 50 (5-10) atmos. over-press. and 250 (160-180) degrees C. A supported Ru catalyst is used. Alkyl gp. may contain 1-5 (1-3) C. Quantitative conversions are achieved. No solvent is used. Highly pure 2-alkyl piperidines are obtd. Catalyst can be re-used, without loss in activity. In an example, 97% pure alpha-Me piperidine was prepd. by hydrogenating alpha-picoline at 10 atmos. over-press., 170 degrees C, using 5% Ru on C as catalyst.
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priorityDate 1975-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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