http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-798412-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-003
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-00
filingDate 1954-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1958-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-798412-A
titleOfInvention Improvements in or relating to the modification and production of titanium ester compounds
abstract A process for chemically modifying a tetra or mixed orthotitanate of the formula Ti(OR)4 or a polymeric titanate of the formula RO[-Ti(OR)2O-]xR, wherein R is an alkyl, aryl, aralkyl or cycloalkyl radical and x is an integer greater than 1, comprises transesterifying such a titanium ester with a carboxylic ester containing a radical in its alcohol-derived portion which is different from at least one organic radical of the titanium ester and containing no free hydroxyl groups to form a product titanium ester different from the reactant titanium ester and a coproduct carboxylic acid ester different from the reactant carboxylic acid ester. In a preferred embodiment a titanium ester of the formula Ti(OR)4, R being an alkyl, aryl, aralkyl or cycloalkyl radical containing at least 6 carbon atoms, for example tetra-octyl titanate, with a carboxylic acid ester of a polybasic alcohol, for example coconut oil, are mixed to form a stable intermediate solution which is heated to form a solid, tough body of glycerol, monoglyceride and diglyceride titanates plasticized by the octyl esters of the coconut acids. The heating may be effected by radiation or baking and temperatures of 50 DEG to 200 DEG C. are suitable. In examples: (1) butyl acetate and tetraisopropyl titanate are reacted and isopropyl acetate is distilled off to leave tetrabutyl titanate; (2) butyl acetate and tetraisopropyl titanate in different proportions are reacted to give diisopropyl dibutyl titanate; (3) reaction of guaiacol acetate and tetraisopropyl titanate give diguaiacol diisopropyl titanate; (4) phenyl benzoate and tetraisopropyl titanate are reacted to form tetraphenyl titanate; (5) a film of a mixture of coconut oil and tetraoctyl titanate is baked at 170 DEG C. on a glass slide to form a solid film; (6) a solid film is formed by heating to 120 DEG C. a xylene solution of a pentaerythritol phthalate resin completely esterified with soya bean acid and tetrastearyl titanate; (7) a xylene solution of an epichlorohydrinbis-phenol copolymer completely esterified with soy acids and tetrastearyl titanate is formed into a solid film by heating at 120 DEG C. on a glass slide, or into a gel by heating at 70 DEG C.; (8) hexaisopropyl dititanate (from the reaction of tetraisopropyl titanate with water) is reacted with benzyl acetate to form tetraisopropyl dibenzyl dititanate.ALSO:A process for chemically modifying a tetra or mixed orthotitanate of the formula Ti(OR)4 or a polymeric titanate of the formula RO[-Ti(OR)2O-]xR wherein R is an alkyl, aryl, aralkyl or cycloalkyl radical and x is an integer greater than 1, comprises transesterifying such a titanium ester with a carboxylic ester containing a radical in its alcohol-derived portion which is different from at least one organic radical of the titanium ester and containing no free hydroxyl groups to form a product titanium ester different from the reactant titanium ester and a co-product carboxylic acid ester different from the reactant carboxylic ester. Among the carboxylic acid esters specified as reactants are polyesters (e.g. glycerol or glycol/phthalic acid polyesters), polymethylmethacrylate, and fatty acid esters such as the soy acids ester of a copolymer of epichlorhydrin and p,p1-biphenol. In examples: (6) a solid film is formed by heating to 120 DEG C. a xylene solution of a pentaerythritol phthalate resin completely esterified with soy bean acid and tetrastearyl titanate; (7) a xylene solution of an epichlorohydrin-bis-phenol copolymer completely esterified with soy acids and tetrastearyl titanate is formed into a solid film by heating to 120 DEG C. on a glass slide, or into a gel by heating at 70 DEG C.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-03080705-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8283437-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7666517-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7750109-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6787632-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6713601-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7767781-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6831138-B2
priorityDate 1953-08-07-04:00^^<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/CID1017
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23963
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414012539
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419486329
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419509663
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7647
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408978442
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419520497
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID110612
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419487220
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID107
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7237
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419531076
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559477
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID3847
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID753
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447829030
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID3847
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419483452
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID84755
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419533389
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID13894
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407364031
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3587356
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID13894
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420229795
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419518430
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454228257
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7835
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13296868
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523117
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID61155
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID757
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21801
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450354738
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID31272
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6589
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID78803
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7169
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393342
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419489467

Total number of triples: 65.