http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101381325-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/C07C231-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C63-04
filingDate 2008-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de998ee7f31b04bf03ce266f56e15b82
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2cb5476c5e4b167883e874cbc882337b
publicationDate 2013-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101381325-B
titleOfInvention Method for simultaneously preparing phenylacetamide and phenylacetic acid by benzyl cyanide hydrolysis in ammonia-containing high temperature aqueous water medium
abstract The invention discloses a method for hydrolyzing phenylacetonitrile in an ammonia-containing high-temperature liquid water medium and preparing phenyl acetamide and phenylacetic acid simultaneously. The method comprises the following steps: 1) deionized water and the phenylacetonitrile with the mass ratio of between 2 to 1 and 8 to 1 are added into a high-pressure reaction kettle, are stirred, and are heated to boil, and an exhaust valve is opened for 2 to 5 minutes; 2) 25 percent ammonia water is pumped through a metering pump to ensure that the ammonia concentration in reactants in the kettle is between 0.05 and 4g/L, and the temperature is increased to be between 180 and 250 DEG C to hydrolyze for 5 to 120 minutes; 3) the temperature is reduced to recover ammonia gas in the kettle; 4) a hydrolysate is cooled, the pH value of the hydrolysate is adjusted to between 8 and 9 , and the hydrolysate is crystallized, and filtered to obtain crude phenyl acetamide; 5) the crude phenyl acetamide is subjected to decolorization by activated carbon, secondary crystallization and vacuum drying to obtain a phenyl acetamide product; and 6) the pH value of filtrate in step 4) is adjusted to between 3 and 4, and the filtrate is crystallized to obtain crude phenylacetic acid, and then the crude phenylacetic acid is subjected to decolorization by the activated carbon, secondary crystallization and vacuum drying to obtain a phenylacetic acid product. The method has a simple and environment-friendly technical process.
priorityDate 2008-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007223920-A
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523291
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1549559
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453034310
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14923
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419588938
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID157161894
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419534234
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7680
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID999
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID516892
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4763
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453595666
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419550829
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14798
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17435
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409060395
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2160
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450926304
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8929
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8794
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448046321
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559581
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419516690
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523755
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22229412
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447607224
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID977
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416129933
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID222
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID297
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419508314
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID294733
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453327643
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419493326
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20083987
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID294733

Total number of triples: 54.