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filingDate 1995-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bea21cd8cf1f4aa03ff6d4e8b455b396
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c55ef29a2dc5f74138b58ff88b4b88f0
publicationDate 1997-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5633407-A
titleOfInvention Process for preparing substituted aromatic amines
abstract A process for preparing substituted aromatic azo compounds is provided which comprises contacting a nucleophilic compound and an azo containing compound in the presence of a suitable solvent system, and reacting the nucleophilic compound and the azo containing compound in the presence of a suitable base and a controlled amount of protic material at a temperature of about 10 DEG C. to about 150 DEG C. in a confined reaction zone wherein the molar ratio of protic material to base is 0:1 to about 5:1. In another embodiment, the substituted aromatic azo compounds are further reacted with a nucleophilic compound in the presence of a suitable solvent system, a suitable base and a controlled amount of protic material at a temperature of about 70 DEG C. to about 200 DEG C. in a confined reaction zone wherein the molar ratio of protic material to base is 0:1 to about 5:1 to produce a substituted aromatic amine. In another embodiment, a process for preparing substituted aromatic amines is provided which comprises contacting a nucleophilic compound and a substituted aromatic azo compound in the presence of a suitable solvent system, and reacting the nucleophilic compound and the substituted aromatic azo compound in the presence of a suitable base and a controlled amount of protic material at a temperature of about 70 DEG C. to about 200 DEG C. in a confined reaction zone wherein the molar ratio of protic material to base is 0:1 to about 5:1. In another embodiment, the substituted aromatic amines of the invention are reductively alkylated to produce alkylated diamines or substituted derivatives thereof.
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226423284
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226420417
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128813338
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226400123
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8127
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127841356
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226444545
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID228304246
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12084
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127840924
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129496528
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128447465
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226450593
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226577365
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226405837
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226416372
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17976294
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129391947
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID347951468
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8093
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID81531

Total number of triples: 316.