http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2543112-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8c6a332c3a115f3ddfabf8db28232bd5 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L2666-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L2666-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L67-04 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09D11-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09J167-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09D17-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09D167-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G63-912 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G63-685 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G63-6854 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G63-914 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09D7-45 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09D7-45 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G63-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K23-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C11D3-00 |
| filingDate | 2012-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f929dfeeaa95dfb602ae799d1275e6d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_339024401d65d7fd3a31c9939e19b4ae http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce081fa216bc1dfc72ced836dd57b521 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_08e3c995f16866ae162050dae17236b3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bd2f385c88a4b12a2e7e04a4c7d64c58 |
| publicationDate | 2015-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2543112-T3 |
| titleOfInvention | Amine adducts that can be prepared by adding Michael |
| abstract | Process for the preparation of an amine adduct, in which the reaction of a polyamine component (A), of a polyester component (B) as well as a hydrocarbon component (C) in weight ratios is carried out from (A): (B)> = 1: 1000 to 1: 1 and (A): (C)> = 1: 100 to 100: 1 so that according to reaction variant i) first of all a a reaction intermediate (AB) is generated from the polyamine component (A) and the polyester component (B), which is then reacted with the hydrocarbon component (C) or according to the reaction variant ii ) Firstly, from the polyamine component (A) and the hydrocarbon component (C) a reaction intermediate (AC) is formed, which is subsequently reacted with the polyester component (B) or according to the reaction variant iii) firstly the polyamine component (A) is reacted at the same time with the poly component ster (B) and the hydrocarbon component (C), wherein the polyester component (B) and the hydrocarbon component (C) do not react with each other under the reaction reaction conditions, the polyamine component (A) It is in the form of organic polyamine compounds (A '), which in each case have at least three amino groups (A' +) selected from primary and secondary amino groups, reactive in each case with the polyester component (B) and the hydrocarbon component (C), the polyester component (B) is in the form of polyester compounds (B '), which in each case do not contain any primary amino group as well as in each case no secondary amino group, present in each case at least three ester groups and in each case contain a coupling group (B '+) present as a carboxyl group or carboxylic acid anhydride group, reactive with primary and / or secondary amino groups and the hydrocarbon component (C) is finds in the form of saturated or unsaturated hydrocarbon compounds (C '), branched or unbranched, which in each case have a linking group (C' +), which do not contain in each case any primary amino group, in each case no secondary amino group, in each case no carboxyl group and in each case no anhydride group of carboxylic acid and in each case have a total relation with respect to carbon atoms in relation to heteroatoms selected from the group of elements O, N, P, S, Si of at minus 2: 1, the linking groups (C '+) presenting in each case the property of reacting with primary amino groups generating secondary amino groups and / or with secondary amino groups forming tertiary amino groups and in each case they are also in form of an activated alkenyl functionality of the general formula (I) R4R5C> = CR6R7 (I) with R4, R5, R6 and R7 in each case independently of each other represented by an electron acceptor substituent E, by H and / or by a r this saturated or unsaturated C1-C12 hydrocarbon, branched or unbranched, with the proviso that in total two of the remains of group R4, R5, R6, R7 can be linked in each case by ring closure with each other, that at minus one of the remains of the group R4, R5, R6, R7 is found as an electron acceptor substituent E and that one of the remains of the group R4, R5, R6, R7 is a bivalent unit, through which the group Binding (C '+) is bonded with the remaining part of the hydrocarbon compound (C'). |
| priorityDate | 2011-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 151.