http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1435621-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3474769a1caadd413cc73787ece4eb42
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-09
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-145
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D309-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-283
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-293
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-48
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-145
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-00
filingDate 1973-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1976-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1435621-A
titleOfInvention Tetra-deca-9,11-dienyl acetate and sex attractant composi tions thereof for insects
abstract 1435621 Tetradeca-9,11-dienyl acetate NATIONAL INSTITUTE OF AGRICULTURAL SCIENCES MINISTRY OF AGRICULTURE & FORESTRY 2 Nov 1973 [14 May 1973] 51083/73 Heading C2C [Also in Division A5] The invention comprises tetradeca-9,11-dienyl acetate and methods of obtaining separate isomers thereof. In Method I, a compound of formula CH#C(CH 2 ) 8 OY, (A), where Y is trimethylsilyl, tetrahydropyran-2-yl (exemplified) or the latter substituted by a C 1 -C 5 alkyl group, is reacted with an alkylmagnesium halide (e.g. C 2 H 6 MgBr) and then with butyraldehyde to give the latter is esterified with p-toluenesulphonyl chloride and acid split off (e.g. with KOH/ ethanol) to give CH 3 CH 2 CH = CHC#C(CH 2 ) 8 OY which is treated with inorganic acid in an alcohol (e.g. H 2 SO 4 in methanol) and then acetylated (with acetic anhydride/pyridine or acetyl chloride/acetic acid) to yield a mixture of the cis and trans isomers of this is hydrogenated using, for example Lindlar's catalyst to give a mixture of the 9-cis/11-cis and 9-cis/11-trans isomers of the claimed compound. The two isomers may be obtained separately by separation by gas chromatography before or after hydrogenation. In Method 2, a compound of formula X<SP>1</SP>Mg(CH 2 ) 7 OY<SP>2</SP> (B), where X<SP>1</SP> is a halogen atom (e.g. Br) and Y is as before (e.g. tetrahydropyranyl), is reacted with where X<SP>11</SP> is halogen (e.g. Br) to obtain a mixture of the cis and trans isomers of which is hydrogenated as before to give a mixture of the 9-cis/11-cis and 9-trans/11-cis isomers of the claimed compound, the separate isomers being obtainable by separation by gas chromotography before or after hydrogenation. By Method III the trans-9/trans-11 isomer is obtained by isomerizing the other isomers, separately or mixed, using, for example as catalyst iodine + sunlight, and separating the product by gas chromatography. Starting material were prepared as follows: A was obtained by the sequence suberic acidmethyl suberate - octanediol - 1 - bromo - 8- hydroxy - octane - 1 - bromo - 8 - tetrahydropyranyl-octane-A. C was obtained by the sequence butyne + acrolein - CH 3 CH 2 C# CHOHCH = CH 2 -C. B was obtained by the sequence -# 1,7 - dihydroxyheptane -# 1- bromo 7 - hydroxy - heptane - 1 - bromo 7- tetrahydroxypyranyl heptanes-B. The compounds are sex-attractants for insects.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-116267931-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-116267931-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2839762-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2403327-A1
priorityDate 1973-05-14-04:00^^<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/CID7918
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID158326025
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12381
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7397
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21225628
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID887
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID176
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393813
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394323
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447629153
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410262431
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID261
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419554831
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425755001
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6367
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410295594
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID93138
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558780
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410066445
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7847
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406903350
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538118
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414927286
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7846
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID807
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449142316
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66284
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411932836
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452325204
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559464

Total number of triples: 56.