http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BG-51516-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_54758b30f0a7334301595435d5f15aa6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_126aa239c80b868bb3e44f6eca221f9b http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_eeb8c96ddeba8d760a5913609b5ce6b3 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-24 |
| filingDate | 1991-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec87c2752511afc5d3f365e5432d56bf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce2b079e3e3c7e5a1f96d86832b2dff2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f77bfba5d87727aa2492cdc442ca40e5 |
| publicationDate | 1993-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | BG-51516-A1 |
| titleOfInvention | Method for the preparation of 2-oxo-1, 3-dioxolan-4-ilmethylacrylate |
| abstract | The method is applicable in the organic synthesis. It avoids the use of poisonous components, such as phosgene and acryloyl chloride. The prepared compound is a monomer in the synthesis of coatings and resists. According to the method, glycidylacrylate interacts with carbon dioxide at a temperature of 70 to 120 degrees C and a pressure of 10 to 50 atm. in the presence of the catalyst alkyl/aryl/ammonium or phosphonic halogenide, which has the formula (R<1>)3R<2>AX, where R<1> is ethyl, butyl or phenyl, R<2> is ethyl, benzyl, butyl or methyl, X is chlorine, bromine or iodine, and A is nitrogen or phosphorus. |
| priorityDate | 1991-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 42.