http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1473119-A

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-685
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-665
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-02
filingDate 1974-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1977-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1473119-A
abstract 1473119 Glycero-phosphoric acid derivatives MAX-PLANCK GES ZUR FORDERUNG DER WISSENSCHAFTEN eV 2 Sept 1974 [6 Sept 1973] 38217/74 Headings C2P and C2C The invention comprises compounds of the general Formula (I) wherein R 1 and R 2 are C 9 to C 17 alkyl and R 3 , R 4 and R 5 are H or CH 3 , and acid addition salts thereof. They are prepared by (a) reacting glycerol with a ketone R 1 C(O)R 2 to form (b) reacting the latter with bromoethyl phosphoric acid dichloride and hydrolysing the product to form and (c) reacting the latter with an aminating agent: (R<SP>3</SP>)(R<SP>4</SP>)NR<SP>5</SP>. Salts may be obtained by mixing stoichiometrically equivalent amounts of the compound (I) and an acid, e.g. HCl, H 2 SO 4 , chloroacetic acid or p-toluene sulphonic acid, in chloroform or other solvent and evaporating to dryness. Step (a) is suitably carried out in an organic solvent (preferably a polar solvent) and in the presence of an acid, e.g. p-toluene sulphonic acid as catalyst and steps (b) and (c) may also be carried out in a polar organic solvent. Water may also be present in step (c). The compounds and their acid addition salts are useful as biodegradable surfactants in detergents and as emulsifiers for foods, e.g. margarine. A glycerol derivative of Formula II in which R 1 and R 2 are each pentadecyl is obtained in Example 1(a) by reacting glycerol with dipentadecyl ketone in benzene in the presence of p-toluene sulphonic acid as catalyst.
priorityDate 1973-09-06-04:00^^<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/CID754
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421057693
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21280451
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6101
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393337
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559219
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID94741
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419581348
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408599808
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419485992
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419483452
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6212
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID177358
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID753
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407563347
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449662972
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID241
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID300
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558313

Total number of triples: 35.