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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C205-37
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-37
filingDate 1978-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e56bdefb320e3f83d3cf085370945978
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80645b74efba74af13ae5fc9f949f676
publicationDate 1980-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4236029-A
titleOfInvention Process for the synthesis of 2,4-dinitro-6-t-butyl-3-methylanisole, referred to as musk ambrette
abstract The invention relates to a process for the synthesis of 2,4-dinitro-6-t-butyl-3-methylanisole or musk ambrette. n The process according to the invention is characterized in that 6-t-butyl-3-methylanisole is reacted with a nitrating mixture consisting of 30 to 50% of acetic acid, 20 to 30% of acetic anhydride and 25 to 45% by weight of nitric acid, at between 7° and 15° C. The product is recovered in the pure state with a good yield by adding small amounts of water to the crude reaction mixture. n Application: Synthesis of a scented product.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2005093670-A1
priorityDate 1977-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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