PROCEDE POUR LA PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE
PROCEDE DE PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE DE FORMULE I, EN FAISANT REAGIR LE (E)-3,7-DIMETHYL-2,6-OCTADIEN-1-OL DE FORMULE II:-SOIT AVEC UN AGENT DE PROPIONATION TEL QUE LE CHLORURE PROPANOIQUE, PUIS UN HYPOHALOGENITE DE BUTYLE TERTIAIRE;-SOIT D'ABORD AVEC L...
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creator | CSABA SZANTAY, LAJOS NOVAK, LASZLO POPPE, BELA MAJOROS, ATTILA KIS-TAMAS, FERENC JURAK ET ISTVAN UJVARY |
description | PROCEDE DE PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE DE FORMULE I, EN FAISANT REAGIR LE (E)-3,7-DIMETHYL-2,6-OCTADIEN-1-OL DE FORMULE II:-SOIT AVEC UN AGENT DE PROPIONATION TEL QUE LE CHLORURE PROPANOIQUE, PUIS UN HYPOHALOGENITE DE BUTYLE TERTIAIRE;-SOIT D'ABORD AVEC L'HYPOHALOGENITE, PUIS AVEC UN AGENT REDUCTEUR ET ENFIN AVEC L'AGENT DE PROPIONATION;-SOIT D'ABORD AVEC UN AGENT ACYLANT, PUIS AVEC DE L'HALOGENITE ET ENFIN AVEC L'AGENT DE PROPIONATION.APPLICATION DE CE COMPOSE DE FORMULE I NOTAMMENT POUR LE TRAITEMENT DES ARBRES FRUITIERS.
A compound of the formula is prepared by a./ reacting /E/-3,7-dimethyl -2,6-octadien-1-ol of the formula /II/ with a propionating agent, preferably propanoic chloride, reacting the propanoate thus obtained with a tert.butyl hypohalide, preferably tert.butyl hypochlorite in a moderately acidic adsorbent, preferably Kieselgel, reacting the halo compound of the general formula /III/ thus obtained wherein R stands for propionyl and Hal represents halogen, with a moderately reactive metal hydride in a polar solvent; or b./ reacting /E/-3,7-dimethyl-2,6-octadien-1-ol of the formula /II/ with a tert.butyl hypohalide, preferably hypochlorite in a moderately polar solvent, in the presence of a moderately acidic adsorbent, preferably Kieselgel, treating the halo compound ofthe general formula /III/, wherein R represents hydrogen and Hal is as defined above, with a reducing agent, reacting the alcohol of the formula /IV/ thus obtained with a propionating agent, preferably propanoic chloride; or c./ converting/E/-3,7-dimethyl-2,6-octadien-1-ol of the formula /II/ with an acylating agent, preferably acetic anhydride, into a compound of the general formula /V/, wherein R is a C1-5 acyl group, adding a tert.butyl hypohalide, preferably tert.butyl hypochlorite, to the C7 double bond thereof in an aprotic, moderately polar solvent, in the presence of a moderately acidic adsorbent, preferably Kieselgel, reducing the compound of the general formula /III/ thus obtained, wherein R is a C1-5 acyl group, with a metal hydride, reacting the alcohol of the formula /IV/ thus obtained with a propionating agent, preferably propanoic chloride; and separating the compound of the formula /I/ thus obtained from the reaction mixture. Traps for destroying male San Jose Scale are baited with the compounds of formula I. |
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fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_FR2542734A1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>FR2542734A1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_FR2542734A13</originalsourceid><addsrcrecordid>eNrjZAgICPJ3dnVxVQjwDw1S8HFUCAhyDXAMcgzx9PdTcAkFcv0DHP38HUNcFYCKNFw1dY11zHVdPH1dQzwifXSNgBx_5xBHF09XP11D3UgfVx4G1rTEnOJUXijNzaDg5hri7KGbWpAfn1pckJicmpdaEu8WZGRqYmRubOJoaEyEEgCW1S2B</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>PROCEDE POUR LA PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE</title><source>esp@cenet</source><creator>CSABA SZANTAY, LAJOS NOVAK, LASZLO POPPE, BELA MAJOROS, ATTILA KIS-TAMAS, FERENC JURAK ET ISTVAN UJVARY</creator><creatorcontrib>CSABA SZANTAY, LAJOS NOVAK, LASZLO POPPE, BELA MAJOROS, ATTILA KIS-TAMAS, FERENC JURAK ET ISTVAN UJVARY</creatorcontrib><description>PROCEDE DE PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE DE FORMULE I, EN FAISANT REAGIR LE (E)-3,7-DIMETHYL-2,6-OCTADIEN-1-OL DE FORMULE II:-SOIT AVEC UN AGENT DE PROPIONATION TEL QUE LE CHLORURE PROPANOIQUE, PUIS UN HYPOHALOGENITE DE BUTYLE TERTIAIRE;-SOIT D'ABORD AVEC L'HYPOHALOGENITE, PUIS AVEC UN AGENT REDUCTEUR ET ENFIN AVEC L'AGENT DE PROPIONATION;-SOIT D'ABORD AVEC UN AGENT ACYLANT, PUIS AVEC DE L'HALOGENITE ET ENFIN AVEC L'AGENT DE PROPIONATION.APPLICATION DE CE COMPOSE DE FORMULE I NOTAMMENT POUR LE TRAITEMENT DES ARBRES FRUITIERS.
A compound of the formula is prepared by a./ reacting /E/-3,7-dimethyl -2,6-octadien-1-ol of the formula /II/ with a propionating agent, preferably propanoic chloride, reacting the propanoate thus obtained with a tert.butyl hypohalide, preferably tert.butyl hypochlorite in a moderately acidic adsorbent, preferably Kieselgel, reacting the halo compound of the general formula /III/ thus obtained wherein R stands for propionyl and Hal represents halogen, with a moderately reactive metal hydride in a polar solvent; or b./ reacting /E/-3,7-dimethyl-2,6-octadien-1-ol of the formula /II/ with a tert.butyl hypohalide, preferably hypochlorite in a moderately polar solvent, in the presence of a moderately acidic adsorbent, preferably Kieselgel, treating the halo compound ofthe general formula /III/, wherein R represents hydrogen and Hal is as defined above, with a reducing agent, reacting the alcohol of the formula /IV/ thus obtained with a propionating agent, preferably propanoic chloride; or c./ converting/E/-3,7-dimethyl-2,6-octadien-1-ol of the formula /II/ with an acylating agent, preferably acetic anhydride, into a compound of the general formula /V/, wherein R is a C1-5 acyl group, adding a tert.butyl hypohalide, preferably tert.butyl hypochlorite, to the C7 double bond thereof in an aprotic, moderately polar solvent, in the presence of a moderately acidic adsorbent, preferably Kieselgel, reducing the compound of the general formula /III/ thus obtained, wherein R is a C1-5 acyl group, with a metal hydride, reacting the alcohol of the formula /IV/ thus obtained with a propionating agent, preferably propanoic chloride; and separating the compound of the formula /I/ thus obtained from the reaction mixture. Traps for destroying male San Jose Scale are baited with the compounds of formula I.</description><language>fre</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1984</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19840921&DB=EPODOC&CC=FR&NR=2542734A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,778,883,25547,76298</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19840921&DB=EPODOC&CC=FR&NR=2542734A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>CSABA SZANTAY, LAJOS NOVAK, LASZLO POPPE, BELA MAJOROS, ATTILA KIS-TAMAS, FERENC JURAK ET ISTVAN UJVARY</creatorcontrib><title>PROCEDE POUR LA PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE</title><description>PROCEDE DE PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE DE FORMULE I, EN FAISANT REAGIR LE (E)-3,7-DIMETHYL-2,6-OCTADIEN-1-OL DE FORMULE II:-SOIT AVEC UN AGENT DE PROPIONATION TEL QUE LE CHLORURE PROPANOIQUE, PUIS UN HYPOHALOGENITE DE BUTYLE TERTIAIRE;-SOIT D'ABORD AVEC L'HYPOHALOGENITE, PUIS AVEC UN AGENT REDUCTEUR ET ENFIN AVEC L'AGENT DE PROPIONATION;-SOIT D'ABORD AVEC UN AGENT ACYLANT, PUIS AVEC DE L'HALOGENITE ET ENFIN AVEC L'AGENT DE PROPIONATION.APPLICATION DE CE COMPOSE DE FORMULE I NOTAMMENT POUR LE TRAITEMENT DES ARBRES FRUITIERS.
A compound of the formula is prepared by a./ reacting /E/-3,7-dimethyl -2,6-octadien-1-ol of the formula /II/ with a propionating agent, preferably propanoic chloride, reacting the propanoate thus obtained with a tert.butyl hypohalide, preferably tert.butyl hypochlorite in a moderately acidic adsorbent, preferably Kieselgel, reacting the halo compound of the general formula /III/ thus obtained wherein R stands for propionyl and Hal represents halogen, with a moderately reactive metal hydride in a polar solvent; or b./ reacting /E/-3,7-dimethyl-2,6-octadien-1-ol of the formula /II/ with a tert.butyl hypohalide, preferably hypochlorite in a moderately polar solvent, in the presence of a moderately acidic adsorbent, preferably Kieselgel, treating the halo compound ofthe general formula /III/, wherein R represents hydrogen and Hal is as defined above, with a reducing agent, reacting the alcohol of the formula /IV/ thus obtained with a propionating agent, preferably propanoic chloride; or c./ converting/E/-3,7-dimethyl-2,6-octadien-1-ol of the formula /II/ with an acylating agent, preferably acetic anhydride, into a compound of the general formula /V/, wherein R is a C1-5 acyl group, adding a tert.butyl hypohalide, preferably tert.butyl hypochlorite, to the C7 double bond thereof in an aprotic, moderately polar solvent, in the presence of a moderately acidic adsorbent, preferably Kieselgel, reducing the compound of the general formula /III/ thus obtained, wherein R is a C1-5 acyl group, with a metal hydride, reacting the alcohol of the formula /IV/ thus obtained with a propionating agent, preferably propanoic chloride; and separating the compound of the formula /I/ thus obtained from the reaction mixture. Traps for destroying male San Jose Scale are baited with the compounds of formula I.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1984</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZAgICPJ3dnVxVQjwDw1S8HFUCAhyDXAMcgzx9PdTcAkFcv0DHP38HUNcFYCKNFw1dY11zHVdPH1dQzwifXSNgBx_5xBHF09XP11D3UgfVx4G1rTEnOJUXijNzaDg5hri7KGbWpAfn1pckJicmpdaEu8WZGRqYmRubOJoaEyEEgCW1S2B</recordid><startdate>19840921</startdate><enddate>19840921</enddate><creator>CSABA SZANTAY, LAJOS NOVAK, LASZLO POPPE, BELA MAJOROS, ATTILA KIS-TAMAS, FERENC JURAK ET ISTVAN UJVARY</creator><scope>EVB</scope></search><sort><creationdate>19840921</creationdate><title>PROCEDE POUR LA PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE</title><author>CSABA SZANTAY, LAJOS NOVAK, LASZLO POPPE, BELA MAJOROS, ATTILA KIS-TAMAS, FERENC JURAK ET ISTVAN UJVARY</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_FR2542734A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>fre</language><creationdate>1984</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>CSABA SZANTAY, LAJOS NOVAK, LASZLO POPPE, BELA MAJOROS, ATTILA KIS-TAMAS, FERENC JURAK ET ISTVAN UJVARY</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>CSABA SZANTAY, LAJOS NOVAK, LASZLO POPPE, BELA MAJOROS, ATTILA KIS-TAMAS, FERENC JURAK ET ISTVAN UJVARY</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PROCEDE POUR LA PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE</title><date>1984-09-21</date><risdate>1984</risdate><abstract>PROCEDE DE PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE DE FORMULE I, EN FAISANT REAGIR LE (E)-3,7-DIMETHYL-2,6-OCTADIEN-1-OL DE FORMULE II:-SOIT AVEC UN AGENT DE PROPIONATION TEL QUE LE CHLORURE PROPANOIQUE, PUIS UN HYPOHALOGENITE DE BUTYLE TERTIAIRE;-SOIT D'ABORD AVEC L'HYPOHALOGENITE, PUIS AVEC UN AGENT REDUCTEUR ET ENFIN AVEC L'AGENT DE PROPIONATION;-SOIT D'ABORD AVEC UN AGENT ACYLANT, PUIS AVEC DE L'HALOGENITE ET ENFIN AVEC L'AGENT DE PROPIONATION.APPLICATION DE CE COMPOSE DE FORMULE I NOTAMMENT POUR LE TRAITEMENT DES ARBRES FRUITIERS.
A compound of the formula is prepared by a./ reacting /E/-3,7-dimethyl -2,6-octadien-1-ol of the formula /II/ with a propionating agent, preferably propanoic chloride, reacting the propanoate thus obtained with a tert.butyl hypohalide, preferably tert.butyl hypochlorite in a moderately acidic adsorbent, preferably Kieselgel, reacting the halo compound of the general formula /III/ thus obtained wherein R stands for propionyl and Hal represents halogen, with a moderately reactive metal hydride in a polar solvent; or b./ reacting /E/-3,7-dimethyl-2,6-octadien-1-ol of the formula /II/ with a tert.butyl hypohalide, preferably hypochlorite in a moderately polar solvent, in the presence of a moderately acidic adsorbent, preferably Kieselgel, treating the halo compound ofthe general formula /III/, wherein R represents hydrogen and Hal is as defined above, with a reducing agent, reacting the alcohol of the formula /IV/ thus obtained with a propionating agent, preferably propanoic chloride; or c./ converting/E/-3,7-dimethyl-2,6-octadien-1-ol of the formula /II/ with an acylating agent, preferably acetic anhydride, into a compound of the general formula /V/, wherein R is a C1-5 acyl group, adding a tert.butyl hypohalide, preferably tert.butyl hypochlorite, to the C7 double bond thereof in an aprotic, moderately polar solvent, in the presence of a moderately acidic adsorbent, preferably Kieselgel, reducing the compound of the general formula /III/ thus obtained, wherein R is a C1-5 acyl group, with a metal hydride, reacting the alcohol of the formula /IV/ thus obtained with a propionating agent, preferably propanoic chloride; and separating the compound of the formula /I/ thus obtained from the reaction mixture. Traps for destroying male San Jose Scale are baited with the compounds of formula I.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | PROCEDE POUR LA PREPARATION DU PROPANOATE DE (E)-3,7-DIMETHYL-2,7-OCTADIEN-1-YLE |
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