Verfahren zur Herstellung von organischen Isocyanaten

An organic a -isocyanato alkyl, aralkyl, aralkenyl or cyclic aliphatic ether is obtained by reacting an a -halogeno-alkyl (-aralkyl, -aralkenyl or -cyclic aliphatic ether with an alkali metal, ammonium, or alkaline earth metal cyanate at 0 DEG to 200 DEG C. in a solvent mixture composed of 0.01 to 8...

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Hauptverfasser: HOLTSCHMIDT HANS, OERTEL GUENTER, ZENNER KARL-FRIEDRICH
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OERTEL GUENTER
ZENNER KARL-FRIEDRICH
description An organic a -isocyanato alkyl, aralkyl, aralkenyl or cyclic aliphatic ether is obtained by reacting an a -halogeno-alkyl (-aralkyl, -aralkenyl or -cyclic aliphatic ether with an alkali metal, ammonium, or alkaline earth metal cyanate at 0 DEG to 200 DEG C. in a solvent mixture composed of 0.01 to 80 volume per cent of a strongly polar solvent as defined below and 99.99 to 20 volume per cent of an aliphatic, cycloaliphatic, araliphatic or aromatic hydrocarbon. The term "strongly polar solvent" refers to a solvent which has a dielectric constant greater than 15 and which does not contain Zerewitinoff-type active hydrogen, e.g. a tertiary amide, carboxylic acid nitrile or a dialkyl dicycloalkyl, aralkyl or diaryl sulphone and several such solvents are specified. Other strongly polar solvents specified are nitroethane, nitropropane, nitrobenzene, nitrotoluene, acetone and acetophenone. The hydrocarbon present in the solvent may be e.g. toluene, benzene, xylene, mesitylene, diethyl benzene, isopropyl benzene, ethyl naphthalene, octane, petroleum ether, gasoline, cyclohexane or methyl cyclohexane. Several examples are given and among the isocyanate products obtainable by the process are those of the general formula R-O-CH(R1)-NCO wherein R is an aralkyl radical, an alkylene radical connected to an O-CH2-NCO group, a Cl-CH2-CH2-radical or CH2=CH-CH2-radical and R1 is a hydrogen atom or an alkyl or aryl radical and the invention includes such products per se as well as the compound C6H5CH.(NCO).O.CH3 formed in one of the examples. Methoxymethyl isocyanate obtainable by the above process can be reacted with O,O-dimethyldithiophosphoryl acetic acid in methylene chloride at 40 DEG C. to form O,O-dimethyl dithiophosphoryl acetic acid N-methoxymethylamide which is effective as an insecticide and acaricide.ALSO:A composition having insecticidal and acaricidal properties is obtained by mixing O,O-dimethyl dithiophosphoryl acetic acid N-methoxymethyl amide with the same amount of dimethyl formamide, adding benzyl hydroxy diphenyl polyglycol ether as emulsifier and then diluting with water.
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The term "strongly polar solvent" refers to a solvent which has a dielectric constant greater than 15 and which does not contain Zerewitinoff-type active hydrogen, e.g. a tertiary amide, carboxylic acid nitrile or a dialkyl dicycloalkyl, aralkyl or diaryl sulphone and several such solvents are specified. Other strongly polar solvents specified are nitroethane, nitropropane, nitrobenzene, nitrotoluene, acetone and acetophenone. The hydrocarbon present in the solvent may be e.g. toluene, benzene, xylene, mesitylene, diethyl benzene, isopropyl benzene, ethyl naphthalene, octane, petroleum ether, gasoline, cyclohexane or methyl cyclohexane. Several examples are given and among the isocyanate products obtainable by the process are those of the general formula R-O-CH(R1)-NCO wherein R is an aralkyl radical, an alkylene radical connected to an O-CH2-NCO group, a Cl-CH2-CH2-radical or CH2=CH-CH2-radical and R1 is a hydrogen atom or an alkyl or aryl radical and the invention includes such products per se as well as the compound C6H5CH.(NCO).O.CH3 formed in one of the examples. Methoxymethyl isocyanate obtainable by the above process can be reacted with O,O-dimethyldithiophosphoryl acetic acid in methylene chloride at 40 DEG C. to form O,O-dimethyl dithiophosphoryl acetic acid N-methoxymethylamide which is effective as an insecticide and acaricide.ALSO:A composition having insecticidal and acaricidal properties is obtained by mixing O,O-dimethyl dithiophosphoryl acetic acid N-methoxymethyl amide with the same amount of dimethyl formamide, adding benzyl hydroxy diphenyl polyglycol ether as emulsifier and then diluting with water.</description><language>ger</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; ADHESIVES ; CHEMICAL PAINT OR INK REMOVERS ; CHEMISTRY ; COATING COMPOSITIONS, e.g. PAINTS, VARNISHES ORLACQUERS ; CORRECTING FLUIDS ; DYES ; FILLING PASTES ; INKS ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; NATURAL RESINS ; ORGANIC CHEMISTRY ; PAINTS ; PASTES OR SOLIDS FOR COLOURING OR PRINTING ; POLISHES ; USE OF MATERIALS THEREFOR ; WOODSTAINS</subject><creationdate>1965</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&amp;date=19651118&amp;DB=EPODOC&amp;CC=DE&amp;NR=1205087B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19651118&amp;DB=EPODOC&amp;CC=DE&amp;NR=1205087B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HOLTSCHMIDT HANS</creatorcontrib><creatorcontrib>OERTEL GUENTER</creatorcontrib><creatorcontrib>ZENNER KARL-FRIEDRICH</creatorcontrib><title>Verfahren zur Herstellung von organischen Isocyanaten</title><description>An organic a -isocyanato alkyl, aralkyl, aralkenyl or cyclic aliphatic ether is obtained by reacting an a -halogeno-alkyl (-aralkyl, -aralkenyl or -cyclic aliphatic ether with an alkali metal, ammonium, or alkaline earth metal cyanate at 0 DEG to 200 DEG C. in a solvent mixture composed of 0.01 to 80 volume per cent of a strongly polar solvent as defined below and 99.99 to 20 volume per cent of an aliphatic, cycloaliphatic, araliphatic or aromatic hydrocarbon. The term "strongly polar solvent" refers to a solvent which has a dielectric constant greater than 15 and which does not contain Zerewitinoff-type active hydrogen, e.g. a tertiary amide, carboxylic acid nitrile or a dialkyl dicycloalkyl, aralkyl or diaryl sulphone and several such solvents are specified. Other strongly polar solvents specified are nitroethane, nitropropane, nitrobenzene, nitrotoluene, acetone and acetophenone. The hydrocarbon present in the solvent may be e.g. toluene, benzene, xylene, mesitylene, diethyl benzene, isopropyl benzene, ethyl naphthalene, octane, petroleum ether, gasoline, cyclohexane or methyl cyclohexane. Several examples are given and among the isocyanate products obtainable by the process are those of the general formula R-O-CH(R1)-NCO wherein R is an aralkyl radical, an alkylene radical connected to an O-CH2-NCO group, a Cl-CH2-CH2-radical or CH2=CH-CH2-radical and R1 is a hydrogen atom or an alkyl or aryl radical and the invention includes such products per se as well as the compound C6H5CH.(NCO).O.CH3 formed in one of the examples. Methoxymethyl isocyanate obtainable by the above process can be reacted with O,O-dimethyldithiophosphoryl acetic acid in methylene chloride at 40 DEG C. to form O,O-dimethyl dithiophosphoryl acetic acid N-methoxymethylamide which is effective as an insecticide and acaricide.ALSO:A composition having insecticidal and acaricidal properties is obtained by mixing O,O-dimethyl dithiophosphoryl acetic acid N-methoxymethyl amide with the same amount of dimethyl formamide, adding benzyl hydroxy diphenyl polyglycol ether as emulsifier and then diluting with water.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>ADHESIVES</subject><subject>CHEMICAL PAINT OR INK REMOVERS</subject><subject>CHEMISTRY</subject><subject>COATING COMPOSITIONS, e.g. PAINTS, VARNISHES ORLACQUERS</subject><subject>CORRECTING FLUIDS</subject><subject>DYES</subject><subject>FILLING PASTES</subject><subject>INKS</subject><subject>METALLURGY</subject><subject>MISCELLANEOUS APPLICATIONS OF MATERIALS</subject><subject>MISCELLANEOUS COMPOSITIONS</subject><subject>NATURAL RESINS</subject><subject>ORGANIC CHEMISTRY</subject><subject>PAINTS</subject><subject>PASTES OR SOLIDS FOR COLOURING OR PRINTING</subject><subject>POLISHES</subject><subject>USE OF MATERIALS THEREFOR</subject><subject>WOODSTAINS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1965</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDANSy1KS8woSs1TqCotUvBILSouSc3JKc1LVyjLz1PIL0pPzMssTs4AynsW5ydXJuYllqTm8TCwpiXmFKfyQmluBnk31xBnD93Ugvz41OKCxOTUvNSSeBdXQyMDUwMLcydjwioA7bMsyQ</recordid><startdate>19651118</startdate><enddate>19651118</enddate><creator>HOLTSCHMIDT HANS</creator><creator>OERTEL GUENTER</creator><creator>ZENNER KARL-FRIEDRICH</creator><scope>EVB</scope></search><sort><creationdate>19651118</creationdate><title>Verfahren zur Herstellung von organischen Isocyanaten</title><author>HOLTSCHMIDT HANS ; OERTEL GUENTER ; ZENNER KARL-FRIEDRICH</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE1205087B3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1965</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>ADHESIVES</topic><topic>CHEMICAL PAINT OR INK REMOVERS</topic><topic>CHEMISTRY</topic><topic>COATING COMPOSITIONS, e.g. PAINTS, VARNISHES ORLACQUERS</topic><topic>CORRECTING FLUIDS</topic><topic>DYES</topic><topic>FILLING PASTES</topic><topic>INKS</topic><topic>METALLURGY</topic><topic>MISCELLANEOUS APPLICATIONS OF MATERIALS</topic><topic>MISCELLANEOUS COMPOSITIONS</topic><topic>NATURAL RESINS</topic><topic>ORGANIC CHEMISTRY</topic><topic>PAINTS</topic><topic>PASTES OR SOLIDS FOR COLOURING OR PRINTING</topic><topic>POLISHES</topic><topic>USE OF MATERIALS THEREFOR</topic><topic>WOODSTAINS</topic><toplevel>online_resources</toplevel><creatorcontrib>HOLTSCHMIDT HANS</creatorcontrib><creatorcontrib>OERTEL GUENTER</creatorcontrib><creatorcontrib>ZENNER KARL-FRIEDRICH</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>HOLTSCHMIDT HANS</au><au>OERTEL GUENTER</au><au>ZENNER KARL-FRIEDRICH</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Verfahren zur Herstellung von organischen Isocyanaten</title><date>1965-11-18</date><risdate>1965</risdate><abstract>An organic a -isocyanato alkyl, aralkyl, aralkenyl or cyclic aliphatic ether is obtained by reacting an a -halogeno-alkyl (-aralkyl, -aralkenyl or -cyclic aliphatic ether with an alkali metal, ammonium, or alkaline earth metal cyanate at 0 DEG to 200 DEG C. in a solvent mixture composed of 0.01 to 80 volume per cent of a strongly polar solvent as defined below and 99.99 to 20 volume per cent of an aliphatic, cycloaliphatic, araliphatic or aromatic hydrocarbon. The term "strongly polar solvent" refers to a solvent which has a dielectric constant greater than 15 and which does not contain Zerewitinoff-type active hydrogen, e.g. a tertiary amide, carboxylic acid nitrile or a dialkyl dicycloalkyl, aralkyl or diaryl sulphone and several such solvents are specified. Other strongly polar solvents specified are nitroethane, nitropropane, nitrobenzene, nitrotoluene, acetone and acetophenone. The hydrocarbon present in the solvent may be e.g. toluene, benzene, xylene, mesitylene, diethyl benzene, isopropyl benzene, ethyl naphthalene, octane, petroleum ether, gasoline, cyclohexane or methyl cyclohexane. Several examples are given and among the isocyanate products obtainable by the process are those of the general formula R-O-CH(R1)-NCO wherein R is an aralkyl radical, an alkylene radical connected to an O-CH2-NCO group, a Cl-CH2-CH2-radical or CH2=CH-CH2-radical and R1 is a hydrogen atom or an alkyl or aryl radical and the invention includes such products per se as well as the compound C6H5CH.(NCO).O.CH3 formed in one of the examples. Methoxymethyl isocyanate obtainable by the above process can be reacted with O,O-dimethyldithiophosphoryl acetic acid in methylene chloride at 40 DEG C. to form O,O-dimethyl dithiophosphoryl acetic acid N-methoxymethylamide which is effective as an insecticide and acaricide.ALSO:A composition having insecticidal and acaricidal properties is obtained by mixing O,O-dimethyl dithiophosphoryl acetic acid N-methoxymethyl amide with the same amount of dimethyl formamide, adding benzyl hydroxy diphenyl polyglycol ether as emulsifier and then diluting with water.</abstract><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
ADHESIVES
CHEMICAL PAINT OR INK REMOVERS
CHEMISTRY
COATING COMPOSITIONS, e.g. PAINTS, VARNISHES ORLACQUERS
CORRECTING FLUIDS
DYES
FILLING PASTES
INKS
METALLURGY
MISCELLANEOUS APPLICATIONS OF MATERIALS
MISCELLANEOUS COMPOSITIONS
NATURAL RESINS
ORGANIC CHEMISTRY
PAINTS
PASTES OR SOLIDS FOR COLOURING OR PRINTING
POLISHES
USE OF MATERIALS THEREFOR
WOODSTAINS
title Verfahren zur Herstellung von organischen Isocyanaten
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