http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002058824-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-42
filingDate 2001-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1c20d5b60f01a903a56904e6b65de23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70402aa3bca1d86b9b8fc09f9b1afb74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffbb4aaabfae1544ebec0a5f2443985a
publicationDate 2002-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002058824-A1
titleOfInvention Solventless synthesis of hydrophilic phenol ester derivatives
abstract Process for preparing benzenesulfonate salts from an appropriately substituted acid chloride and a hydroxybenzenesulfonic acid is conducted in the absence of solvent, in a molar excess of acid chloride and in the presence of a phase transfer catalyst selected from quaternary ammonium and quaternary phosphonium salts and the target reaction product. The molar excess of the acid chloride is used to reduce the occurrence of gelation in the product.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6822113-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004019229-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6864381-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2019284392-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004198995-A1
priorityDate 2000-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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