PRODUCTION OF 3-METHYL-1-BUTENE
1,192,578. Olefins. PHILLIPS PETROLEUM CO. 18 Sept., 1967 [19 Sept., 1966], No. 42409/67. Heading C5E. 3-Methyl-1-butene is prepared by catalytically dimerizing propylene to obtain at least some 4- methyl-2-pentene, which is then contacted with ethylene in the presence of an olefin disproportionatio...
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description | 1,192,578. Olefins. PHILLIPS PETROLEUM CO. 18 Sept., 1967 [19 Sept., 1966], No. 42409/67. Heading C5E. 3-Methyl-1-butene is prepared by catalytically dimerizing propylene to obtain at least some 4- methyl-2-pentene, which is then contacted with ethylene in the presence of an olefin disproportionation catalyst to produce 3-methyl-1-butene as desired product and propylene, which may be recycled to the dimerization. Other products of the dimerization may be treated as follows. 4-methyl-1-pentene may be recovered as product by fractionation, or may be isomerized to 4-methyl-2-pentene which is fed to the disproportionation. 2 - Methyl - 2 - and - 1 - pentenes may be recovered as products by fractionation and, either removed from the process, or may be isomerized to additional 4-methyl-2-pentene which is fed to the disproportionation. Suitable catalysts for the various reactions are: Dimerization: tripropyl aluminium, Na/K alloy, or #-allyl nickel iodide/triphenyl phosphine/ethyl aluminium dichloride. Disproportionation: an oxide of Mo, W or Re, or a hexacarbonyl or sulphide of W or Mo, any of which may be supported on SiO 2 , Al 2 O 3 , SiO 2 /Al 2 O 3 , MgO/TiO 2 , ZrO 2 , ThO 2 , AlP0 4 or ZrP0 4 , and may contain additives such as CoO or K 2 C0 3 . Isomerization: MgO, Al 2 O 3 , SiO 2 , CoO, FeO or MnO. Unconverted reactants or undesired products from any stage of the process may be recycled to any other appropriate stage. |
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Heading C5E. 3-Methyl-1-butene is prepared by catalytically dimerizing propylene to obtain at least some 4- methyl-2-pentene, which is then contacted with ethylene in the presence of an olefin disproportionation catalyst to produce 3-methyl-1-butene as desired product and propylene, which may be recycled to the dimerization. Other products of the dimerization may be treated as follows. 4-methyl-1-pentene may be recovered as product by fractionation, or may be isomerized to 4-methyl-2-pentene which is fed to the disproportionation. 2 - Methyl - 2 - and - 1 - pentenes may be recovered as products by fractionation and, either removed from the process, or may be isomerized to additional 4-methyl-2-pentene which is fed to the disproportionation. Suitable catalysts for the various reactions are: Dimerization: tripropyl aluminium, Na/K alloy, or #-allyl nickel iodide/triphenyl phosphine/ethyl aluminium dichloride. Disproportionation: an oxide of Mo, W or Re, or a hexacarbonyl or sulphide of W or Mo, any of which may be supported on SiO 2 , Al 2 O 3 , SiO 2 /Al 2 O 3 , MgO/TiO 2 , ZrO 2 , ThO 2 , AlP0 4 or ZrP0 4 , and may contain additives such as CoO or K 2 C0 3 . Isomerization: MgO, Al 2 O 3 , SiO 2 , CoO, FeO or MnO. 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CRAIN</creatorcontrib><creatorcontrib>PAUL R. STAPP</creatorcontrib><title>PRODUCTION OF 3-METHYL-1-BUTENE</title><description>1,192,578. Olefins. PHILLIPS PETROLEUM CO. 18 Sept., 1967 [19 Sept., 1966], No. 42409/67. Heading C5E. 3-Methyl-1-butene is prepared by catalytically dimerizing propylene to obtain at least some 4- methyl-2-pentene, which is then contacted with ethylene in the presence of an olefin disproportionation catalyst to produce 3-methyl-1-butene as desired product and propylene, which may be recycled to the dimerization. Other products of the dimerization may be treated as follows. 4-methyl-1-pentene may be recovered as product by fractionation, or may be isomerized to 4-methyl-2-pentene which is fed to the disproportionation. 2 - Methyl - 2 - and - 1 - pentenes may be recovered as products by fractionation and, either removed from the process, or may be isomerized to additional 4-methyl-2-pentene which is fed to the disproportionation. Suitable catalysts for the various reactions are: Dimerization: tripropyl aluminium, Na/K alloy, or #-allyl nickel iodide/triphenyl phosphine/ethyl aluminium dichloride. Disproportionation: an oxide of Mo, W or Re, or a hexacarbonyl or sulphide of W or Mo, any of which may be supported on SiO 2 , Al 2 O 3 , SiO 2 /Al 2 O 3 , MgO/TiO 2 , ZrO 2 , ThO 2 , AlP0 4 or ZrP0 4 , and may contain additives such as CoO or K 2 C0 3 . Isomerization: MgO, Al 2 O 3 , SiO 2 , CoO, FeO or MnO. Unconverted reactants or undesired products from any stage of the process may be recycled to any other appropriate stage.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1969</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJAPCPJ3CXUO8fT3U_B3UzDW9XUN8Yj00TXUdQoNcfVz5WFgTUvMKU7lhdLcDPJuriHOHrqpBfnxqcUFicmpeakl8aHBxiam5sZGBo7GhFUAAETWIL0</recordid><startdate>19690722</startdate><enddate>19690722</enddate><creator>DONALD L. CRAIN</creator><creator>PAUL R. STAPP</creator><scope>EVB</scope></search><sort><creationdate>19690722</creationdate><title>PRODUCTION OF 3-METHYL-1-BUTENE</title><author>DONALD L. CRAIN ; PAUL R. STAPP</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US3457320A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1969</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>DONALD L. CRAIN</creatorcontrib><creatorcontrib>PAUL R. STAPP</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>DONALD L. CRAIN</au><au>PAUL R. STAPP</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PRODUCTION OF 3-METHYL-1-BUTENE</title><date>1969-07-22</date><risdate>1969</risdate><abstract>1,192,578. Olefins. PHILLIPS PETROLEUM CO. 18 Sept., 1967 [19 Sept., 1966], No. 42409/67. Heading C5E. 3-Methyl-1-butene is prepared by catalytically dimerizing propylene to obtain at least some 4- methyl-2-pentene, which is then contacted with ethylene in the presence of an olefin disproportionation catalyst to produce 3-methyl-1-butene as desired product and propylene, which may be recycled to the dimerization. Other products of the dimerization may be treated as follows. 4-methyl-1-pentene may be recovered as product by fractionation, or may be isomerized to 4-methyl-2-pentene which is fed to the disproportionation. 2 - Methyl - 2 - and - 1 - pentenes may be recovered as products by fractionation and, either removed from the process, or may be isomerized to additional 4-methyl-2-pentene which is fed to the disproportionation. Suitable catalysts for the various reactions are: Dimerization: tripropyl aluminium, Na/K alloy, or #-allyl nickel iodide/triphenyl phosphine/ethyl aluminium dichloride. Disproportionation: an oxide of Mo, W or Re, or a hexacarbonyl or sulphide of W or Mo, any of which may be supported on SiO 2 , Al 2 O 3 , SiO 2 /Al 2 O 3 , MgO/TiO 2 , ZrO 2 , ThO 2 , AlP0 4 or ZrP0 4 , and may contain additives such as CoO or K 2 C0 3 . Isomerization: MgO, Al 2 O 3 , SiO 2 , CoO, FeO or MnO. Unconverted reactants or undesired products from any stage of the process may be recycled to any other appropriate stage.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY COMPOSITIONS BASED THEREON MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS METALLURGY ORGANIC CHEMISTRY ORGANIC MACROMOLECULAR COMPOUNDS THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | PRODUCTION OF 3-METHYL-1-BUTENE |
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