http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20120016313-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7f512d368dd6c66907c5f306f2b79d15
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D303-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D303-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-16
filingDate 2010-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b65fe18d9ad9beaabdafd276abe139a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_095b7c822535066e1aba00f19edfd667
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0903488cf4df8e8442fdf687662042cb
publicationDate 2012-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20120016313-A
titleOfInvention Process for preparing glycidyl esters of branched monocarboxylic acids
abstract The present invention relates to aliphatic monocarboxylic acids represented by the formula R 1 R 2 R 3 COOH, wherein R 1 , R 2 and R 3 each independently represent an alkyl radical having a normal or branched structure containing 1 to 20 carbon atoms. And an epoxyalkyl halide containing 3 to 13 carbon atoms in the presence of a catalyst, wherein more than stoichiometric amounts of the epoxyalkyl halide are reacted with an acid (eg, preferably in the range 1.02: 1 to 1.50: 1). Molar ratio of epoxyalkyl halide to acid) to form an intermediate reaction product containing halohydrin, which is added to the acid with moderate cooling of the reactant / reaction mixture to maintain the temperature of the reaction mixture below 80 ° C. Then, the epoxyalkyl halide and the acid are sufficient to reduce the amount of acid to 2 wt% or less and 0.1 wt% or more based on the initial acid amount. Reacting at a temperature of less than 80 ° C. (preferably in the range of 55 to 75 ° C.) during the liver, optionally removing any excess epoxyalkyl halide from the reaction product before the ring closure reaction, subjecting the reaction product to a ring closure reaction To a process for preparing glycidyl esters of branched monocarboxylic acids by treatment with (DHC) and optionally with at least one post-treatment (ADHC) to remove any remaining halo functional groups.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101650528-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10954206-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017171329-A1
priorityDate 2009-06-11-04:00^^<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/substance/SID454340979
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451486588
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426384635
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559213
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413930116
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425823261
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10430
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419586842
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID448893
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15564205
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451216657
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412076115
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10920443
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411832430
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419526858
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6915
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448400546
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457623688
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408978443
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456028012
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86696089
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21377
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6590
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452694252
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24341
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID78474
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12449
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410627549
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412048349
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453556179
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66137
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415731135
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454474765
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6950109
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8697
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7413
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559516
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7289
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID101416667
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397365
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID260
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419520307
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID62817
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6379

Total number of triples: 65.