http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110156613-B

Outgoing Links

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-582
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C213-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C213-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-22
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-10
filingDate 2019-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110156613-B
titleOfInvention A kind of synthetic method of 3,3-diaminobiphenol hydrochloride
abstract The invention provides a method for synthesizing 3,3-diaminobiphenol hydrochloride. The method for synthesizing is as follows: adding raw material 4,4-biphenol and a reaction solvent into a reaction vessel, stirring, and dropping in an ice bath Add concentrated nitric acid, carry out nitration reaction under ice bath for 1~4h after the dropwise addition, and then after post-treatment to obtain intermediate 3,3-dinitrobiphenol; add 3,3-dinitrobiphenol into the reaction vessel , activated carbon, ferrous sulfate heptahydrate, anhydrous ethanol, reflux at 80°C, dropwise add hydrazine hydrate, carry out reduction reaction under reflux for 7-12h after dropwise addition, and then the reaction solution is post-treated to obtain product 3,3-di Amino biphenol hydrochloride; the reaction process parameters of the invention are easy to control, less energy consumption, no generation of highly toxic by-products, good yield, high purity, and high industrial feasibility.
priorityDate 2019-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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