Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d648658dd620f548c24de39659a5e9e3 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2531-842 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-003 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-013 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2231-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2540-10 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-39 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2295 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F15-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-44 |
classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-013 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-003 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-39 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22 |
filingDate |
2018-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
2020-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_655d46741a9c41470f2423c97087837a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82dcb450cb4fed4cbf943ff4a1e82517 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4c2723084ec8f4d86fdd5a3055af864 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be02ef2da278b56cf65c04a911315eac |
publicationDate |
2020-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-10590062-B1 |
titleOfInvention |
Iron-catalyzed selective production of methyl esters from aldehydes |
abstract |
A process for making methyl esters in high yields is provided. The process comprises contacting aliphatic or aromatic aldehydes and methanol with an iron catalyst, to catalyze the dehydrogenative coupling between aliphatic or aromatic aldehydes and methanol. The reaction is highly selective (<99.9%) toward the formation of methyl esters over homoesters and alcohols and operates at temperatures of less than 100° C. for 2-8 hours. |
priorityDate |
2018-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |