http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2303784-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d9cb217f83556ce2a418344c2d485415
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J27-1802
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J27-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-18
filingDate 1976-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1976-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2303784-A1
titleOfInvention PROCESS FOR THE PREPARATION OF DIPHENOL MONOALCOYL ETHERS
abstract Bivalent phenol (opt. substd. with 1-4C lower alkyl or halogen, e.g. catechol, hydroquinone, resorcin, etc.) is subjected to etherification with a lower alcohol (straight-chained or branched aliphatic lower alcohol of 1-4C, e.g. methanol, ethanol, isobutano, etc.) in the presence of a catalyst consisting of aluminium and phosphor in a gaseous phase, and by the addn. of a very small amt. of boron phosphate (30-500 p.p.m. relative to the mixt. soln. of bivalent phenol and alcohol), not only is it possible to prevent the formation of a tar-like substance to some extent but also to maintain a high catalytic activity and selectivity for a long period of time, which is very advantageous on an industrial scale. For example, in the prodn. of guaiacol, the selectivity of veratrol, whose b.pt. is very similar to that of guaiacol (the difference is 1-2 degrees C), which cannot be sepd. by distillation, is not higher than 1%, thus this is very advantageous from the viewpoint of sepn. and purificn.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0420756-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0420756-A3
priorityDate 1975-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID887
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5054
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7043
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID996
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419491804
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419522477
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419474313
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5359268
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419474383
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419474448
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407327152
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558575
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID460
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24404
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559532
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID785
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454436140
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411932836
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID289

Total number of triples: 34.