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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C317-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C317-48
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-48
filingDate 1990-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf95dfd3620cda4ab859610747fcfe3d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_337a2e7acd77e25379d837cfe11b5020
publicationDate 1991-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5043469-A
titleOfInvention Process for preparing 5-substituted aminophenols
abstract Process for the introduction of functional or functionalizable substituents para to the amino group in 2-aminophenols and 3-aminophenols. The process proceeds in one step, with substitution occurring selectively at the position para to the amino group. Consequently, the reaction is surprisingly straightforward, with very little or no contamination by isomeric by-products. The process comprises reaction of (a) an aminophenol having an open para position to the amino function, with (b) an unhindered non-enolizable aldehyde, and (c) a thiol or sulfinic acid which acts as a nucleophile. In preferred embodiments, the process is conducted at a temperature of from about 50 DEG C. to about 100 DEG C., and in the presence of a polar solvent. The reaction is promoted by an acid having sufficient acidity to protonate the amino group of the aminophenol. Preferably, the acid promoter is a mineral acid, and it is present in an amount at least substantially equivalent to the amount of aminophenol reactant. The promoter can be added as a salt of the aminophenol.
priorityDate 1989-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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