http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2014121390-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-08
filingDate 2014-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3772e33f99c6665f365aba3e28b305d0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aef24a2af3286650425949d448537359
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1dafb0bff8756cdc0b9f9d4bdfb9307c
publicationDate 2014-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2014121390-A1
titleOfInvention Method for producing tetrahydrofuran
abstract The present invention relates to a method for producing tetrahydrofuran comprising: feeding raw material 1,4-butanediol containing gamma butyrolactone to a reaction tank, and performing a dehydration cyclization reaction in the presence of a homogeneous acid catalyst having a pKa of 4 or less and being dissolvable in 1,4-butanediol to produce tetrahydrofuran, wherein a gas containing tetrahydrofuran, gamma butyrolactone and water in the reaction tank is introduced into a heat exchanger and when obtaining a condensate from the outlet of the heat exchanger, the ratio of the concentration of gamma butyrolactone in the condensate based on the concentration of gamma butyrolactone in the raw material 1,4-butanediol is from 20 to 100%.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114702465-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9873652-B2
priorityDate 2011-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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