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filingDate 1988-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9760307052477bb75e583e75204197e0
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publicationDate 1989-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01311087-A
titleOfInvention Production of phosphatidylcholine
abstract PURPOSE: To contrive simplification and high yield in a reaction process of the subject compound useful as cosmetics and medicines by reacting glycerophosphocholine with an acyl chloride in the presence of hexamethylphosphoric triamide. n CONSTITUTION: For example, in the presence of 10-40mol equivalents hexamethylphosphoric triamide (preferably dehydrated by an addition of molecular sieves in use) as a reaction solvent as well as a proton acceptor, 1mol equivalent dry glycerophosphocholine (obtained from a native phosphatidylcholine by deacylation) is dispersed and 1.6-6mol equivalents acylchloride (one without causing isomerization at an aliphatic or aromatic site) are added thereto and the reaction is carried out preferably at 40-60°C for 1-3hr, followed by purification of the resultant reaction product by silicic acid column chromatography with a gradient chloroform/methanol to afford the aimed compound. n COPYRIGHT: (C)1989,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0609078-A1
priorityDate 1988-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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