http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102432487-B

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d6a6f422b091ba12ea61d4adbf1b0e8e
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-25
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-15
filingDate 2011-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99303dd9579344531bbc94c92b44640c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4cf84e4c86033a08c6436df0fe3b4c6e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00fb79c1eef97da2fddd59fdd736b980
publicationDate 2014-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102432487-B
titleOfInvention Catalysis-based amino acetylation method
abstract The invention discloses a catalysis-based amino acetylation method. The catalysis-based amino acetylation method utilizes Lewis alkali ionic liquid [HDBU]OAc as a catalyst, acetic anhydride as an acetylation agent, and an alicyclic amine or an aromatic amine as a substrate. The catalysis-based amino acetylation method comprises the following steps that 1, the substrate undergoes an acetylation reaction in the dis-presence of a solvent at a temperature of 40 to 80 DEG C for 0.3 to 1.5 hours, wherein a mole ratio of acetic anhydride to the substrate is (1.0 to 2.0): 1 and a mole ratio of Lewis alkali ionic liquid [HDBU]OAc to the substrate is in a range of 10 to 30%; 2, after the acetylation reaction, ether is added into the products; 3, the mixture obtained by the step 2 is filtered and separated; 4, the supernatant extract obtained by the step 3 is washed orderly through a saturated NaHCO3 solution and water; 5, the washed supernatant extract is added with waterless Na2SO4 for drying; and 6, the ether is removed by reduced pressure rotary distillation so that a finished product is obtained. The catalysis-based amino acetylation method has the characteristics of wild reaction conditions, high yield, low cost, environmental benefits and high safety.
priorityDate 2011-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458395511
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419488072
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419484514
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12084
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450136125
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424468172
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424356992
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7468
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID176
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7615
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24341
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419517283
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453034310
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6373
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419526858
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6946
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7504
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9731
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10824
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419518845
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559261
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419543712
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406903350
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419546198
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7965
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458396401
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6922
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421468374
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3283
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414862405
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419585359
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7684
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7475
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7242
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID516892
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424352925
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8007
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7918
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411558826
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558780
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID121825
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419517244

Total number of triples: 62.