http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1558902-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C391-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C391-00
filingDate 1988-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ade6a37a50eafc36b8687845415f273
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc45f6bb747fcb83bae469d8119ae1b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5fd79afedcdedbf696cf114547fa22ce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd8a556f171dda252571b11cf2cb2bcb
publicationDate 1990-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1558902-A1
titleOfInvention Method of obtaining 1-(organylthio)-2-chloro-2(organylseleno)ethers
abstract The invention relates to organic selenium derivatives, in particular the preparation of 1- (organylthio) -2-chloro-2 (organic seleno) -ethenes of a common f-ly: RSCH = C (CI) SER 1 , where a) R = C 2 H 5 n n n R 1 = C 6 H 5 n n n b) R = iso-C 3 H 7 n n n R 1 = C 6 H 5 n n n c) R = HC 4 H 9 n n n R 1 = C 6 H 5 n n n g) R = C 2 H 5 n n n R 1 = HC 4 H 9 , which can be used as starting compounds for the preparation of biologically active substances and reagents for fine organic synthesis. The goal is to create a new one-step method for obtaining new compounds. The synthesis is carried out by the reaction of the corresponding organic thiochloride acetylenes with the organic selenols at their equimolar ratio in diethyl ether medium at 20-22 ° C for 6 hours. Yield,%n n n bp, ° Cn n n gross l a) 47n n n 142-145n n n C 10 H 11 CLSSEn n n b) 78n n n 126-132n n n C 11 H 14 CLSSEn n n c) 80n n n 160-165n n n C 12 H 15 CLSSEn n n d) 35-82n n n 123-125n n n C 8 H 15 CLSSE.
priorityDate 1988-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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