Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_169b5fab2d1d1fe7f8d456e4327d6aeb http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2efbe95965e682e179dfd266c9980505 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_de2491de13a2c6f8c3a2b6f5c0b50fb8 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-93 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C59-185 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-00 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-185 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-93 |
filingDate |
2011-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c3e366ab12d26f6f8cb2a3c8d6d89d7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad605410d1a06872b20b11bd2a77a0d8 |
publicationDate |
2013-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-2013123520-A1 |
titleOfInvention |
Microwave assisted synthesis of dehydrated sugar derivatives hydroxymethylfurfural, levulinic acid, anhydrosugar alcohols, and ethers thereof |
abstract |
Methods for the production of dehydrated sugars and derivatives of dehydrated sugars using microwave (MW) irradiation and methods of purifying the same are described. The dehydrated sugars derivatives include 5-hydroxymethyl-2-furfural (HMF) and anhydrosugar alcohols such as sorbitans and isosorbide. The derivatives include HMF ethers, levulinic acid esters, and ether derivatives of the anhydrosugar alcohols. The described methods require lower reaction temperatures and shorter reaction times than similar non microwave mediated reactions known in the art. Typical reaction conditions are 120-210° C., and typical reaction times are 30 minutes or less. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108473455-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107108645-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114315768-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10023586-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3114230-A4 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017501988-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015094895-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015094894-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2015224247-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015134557-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016099789-A1 |
priorityDate |
2010-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |