http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-3037086-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bcd600c789c13101f39db5af4f289a97
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-02
filingDate 1980-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b97279cecbb8fcfb024d2188143c108
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7eb2ce50b7fa25948caa886d32a35321
publicationDate 1982-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-3037086-A1
titleOfInvention 3- (M-CHLORANILINO-) ACRYLIC ACID ETHYL ESTER AND A METHOD FOR THE PRODUCTION THEREOF
abstract 3-(m-Chloroanilino)acrylic acid ethyl ester (I) is new. (I) is an intermediate for 4-hydroxy-7-chloroquinoline, which in turn is a precursor of antimalarials of the chloroquine type. (I) is prepd. by reaction of m-chloroaniline with sodium 3-hydroxy-acrylic acid ethyl ester in a water/alcohol solvent mixt. in the presence of a mineral acid or acetic acid. Pref. alcohols for use as solvents are 1-4C alcohols, esp. MeOH or EtOH, or ether alcohols such as methyl glycol. The ratio of alcohol to water at the end of the reaction is pref. 10:1 to 1:5, esp. 5:1 to 1:2 v/v. Reaction temp. is pref. minus 25 to plus 25 deg.C.; the trans-isomer of (I) is formed preferentially when the reaction temp. is minus 25 to plus 25 deg.C., esp. minus 10 to plus 10 deg.C.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7601864-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101020647-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4910327-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0217018-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0388744-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4772711-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-3531067-A1
priorityDate 1980-10-01-04:00^^<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/compound/CID176
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426228520
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8019
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5360545
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559553
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414859283
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID428565860
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3283
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411282759
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24196931
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421993527
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410281913
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559261
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2719
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6547
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7932
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66593
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449603119
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411932836
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13351308
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419504623
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419487010
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID75234047
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19096565
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447917231
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406903350
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID887
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16723172

Total number of triples: 51.