http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-739907-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2fa8f8941ecc2d9521285617dbb93322
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C37-86
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C37-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-19
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-08
filingDate 1952-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10457c7659872908a1e05fb53a14a57d
publicationDate 1955-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-739907-A
titleOfInvention Recovery of phenols
abstract A process for the production of resorcinol by the catalytic cleavage of a reaction mixture containing meta-di-isopropylbenzene hydroperoxide derived from the oxidation of meta-di-isopropylbenzene comprises decomposing by the action of heat the material contained in the cleavage reaction product which is less volatile than resorcinol and recovering the additional quantities of resorcinol and the meta-isopropenylphenol so formed. The heat treatment may be conducted in presence of an acid catalyst or, alternatively, the cleavage reaction product is treated to remove or neutralize cleavage catalysts and stripped of low-boiling materials before being subjected to heat treatment. The heat treatment is also preferably conducted at 200-400 DEG C. at super- or sub-atmospheric pressures and in presence of a high-boiling inert diluent (preferably boiling at or above 200 DEG C., e.g. tri-isopropyl- or 1 : 2 : 4-trichlorobenzene; isopropyl-, methyl-, chloro- or bromonaphthalene; a gas oil fraction; or a mixture thereof), the heat-treated cleavage reaction product being distilled and the resorcinol and meta-isopropenylphenol recovered from the distillate preferably by crystallization and filtration, or by distilling directly into water. The heat treatment and distillation are preferably conducted simultaneously, and the proportion of high-boiling inert diluent is preferably adjusted so that the distillate is not saturated with respect to resorcinol while still above the temperature at which crystallization takes place. Further quantities of resorcinol may be recovered from solution in the inert diluent mother-liquors by extraction with water; meta-isopropenylphenol is also recovered by extracting the resorcinol-free inert diluent with an aqueous alkaline solution. Mixed resorcinol/meta-isopropenylphenol phases are separated (1) by extraction with a solvent, e.g. benzene, toluene, methyl-naphthalene, chloroform or carbon tetrachloride; or (2) by partition between two immiscible solvents, e.g. water and one of the solvents in (1). The resorcinol, after separation from the meta-isopropenyl phenol, may be further purified by redistillation, or by sublimation.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2404615-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0280403-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4192958-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9105755-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-115636913-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4239921-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4283567-A
priorityDate 1952-09-10-04:00^^<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/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1140
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419474448
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421316343
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6278
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419514042
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419474313
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7001
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408288535
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID996
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7002
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7003
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419527201
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559219
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5943
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5054
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID241
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412734083
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22535
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419527288
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456922693

Total number of triples: 42.