http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2752408-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-02
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-02
filingDate 2011-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_027d5951b2b69dd1bfdd5f6308d841f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04ae9f7ac2ea01ee2645a35d3e41515a
publicationDate 2014-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2752408-A1
titleOfInvention Preparation of aminomethyl furans and alkoxymethyl furan derivatives from carbohydrates
abstract Described herein are single step methods of making various classes of alkylamine derivatives of furan and tetrahydrofuran by simultaneous contact of a sugar with H 2 , an acid catalyst and hydrogenation catalyst in the presence of an alkylamide solvent. The hydrogenation catalyst is a heterogeneous catalyst comprising a metal selected from the group consisting of Pt, Pd, and nickel. The acid catalysts may be homogeneous mineral acid or a heterogeneous acid catalyst on substrate. In a preferred practice the two catalysts are provided on a common heterogeneous bifunctional support. Using similar combinations of acid and hydrogenation catalysts, there is also described single step methods for making furandimethanol by simultaneously contacting a hexose with the two separate catalysts in the presence of H 2 in an aprotic solvent, such as dimethylformamide. With the same catalyst system and similar reaction conditions, 2, 5 furan dialkylethers can also be made in a single step when the solvent includes an ROH alcohol.
priorityDate 2010-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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