Dimerization method of lower olefins and alcohol production with dimerized products

{
  "publication_number": "US5446213A",
  "country": "US",
  "kind": "A",
  "title": "Dimerization method of lower olefins and alcohol production with dimerized products",
  "abstract": "PCT No. PCT/JP93/01425 Sec. 371 Date Jun. 3, 1994 Sec. 102(e) Date Jun. 3, 1994 PCT Filed Oct. 5, 1993.The present invention is directed to a method of dimerizing lower olefins which comprises dimerizing a lower olefins in the presence of a catalyst, wherein the catalyst used comprises a nickel compound, an organic aluminum compound, and a phosphite compound having the general formula (I): (I) wherein R1, R2, R3, and R4are phenyl groups optionally substituted by substituents and may be different from each other, at least two of R1, R2, R3, and R4 have a hydrocarbon group as a substituent in the ortho position; A is a divalent aliphatic, alicyclic or aromatic hydrocarbon group which optionally has a substituent; and n is 0 or 1. The present invention is also directed a method of producing alcohol by means of hydroformylating and hydrogenating the newly formed olefins obtained through the said dimerization method of the lower olefins. In the dimerization method of the lower olefins according to the present invention, it is possible to produce in an economic manner olefinic mixtures which are high in activity and low in degree of branching. In addition, the alcohols produced with the said olefins show totally superior performance as the raw material for plasticizers, which are thus valuable in industrial applications.",
  "claims": [
    "1. A method of dimerizing lower olefins which comprises dimerizing a lower olefin in the presence of a catalyst, wherein the catalyst used comprises a nickel compound, an organic aluminum compound, and a phosphite compound having the general formula (I): ##STR32## wherein R 1, R 2, R 3, and R 4 are phenyl groups optionally substituted by substituents and may be different from each other, at least two of R 1, R 2, R 3, and R 4 have a hydrocarbon group as a substituent in the ortho position; A is a divalent aliphatic, alicyclic or aromatic hydrocarbon group which optionally has a substituent; and n is 0 or 1.",
    "2. A method as claimed in claim 1, wherein the lower olefin is a butene.",
    "3. A method as claimed in claim 1, wherein the nickel compound is a nickel carboxylate.",
    "4. A method as claimed in claim 1, wherein the nickel compound is a complex compound of nickel.",
    "5. A method as claimed in claim 1, wherein the organic aluminum compound is a halogenated alkylaluminum compound.",
    "6. A method as claimed in claim 1, wherein the hydrocarbon groups which at least two of R 1, R 2, R 3, and R 4 in the phosphite compound having the general formula (I) have as a substituent in the ortho position, are alkyl groups.",
    "7. A method as claimed in claim 1, wherein n in the phosphite compound having the general formula (I) is equal to zero.",
    "8. A method as claimed in claim 7, wherein all of R 1, R 2, and R 3 in the phosphite compound having the general formula (I) have a hydrocarbon group as the substituent in the ortho position.",
    "9. A method as claimed in claim 1, wherein n in the phosphite compound having the general formula (I) is equal to one.",
    "10. A method as claimed in claim 9, wherein all of R 1, R 2, R 3, and R 4 in the phosphite compound having the general formula (I) have a hydrocarbon group as the substituent in the ortho position.",
    "11. A method as claimed in claim 9, wherein the group A in the phosphite compound having the general formula (I) is a divalent aliphatic hydrocarbon group having from 2 to carbon atoms.",
    "12. A method as claimed in claim 9, wherein the group A in the phosphite compound having the general formula (I) is an alicyclic hydrocarbon group having from 4 to 12 carbon atoms.",
    "13. A method as claimed in claim 9, wherein the group A in the phosphite compound having the general formula (I) is an aromatic hydrocarbon group having from 6 to 12 carbon atoms.",
    "14. A method as claimed in claim 9, wherein the group A in the phosphite compound having the general formula (I) is represented by --R--B--R-- wherein R is a divalent aliphatic hydrocarbon group, a divalent alicyclic hydrocarbon group or a divalent aromatic hydrocarbon group, which is optionally substituted by an alkyl group having from 1 to 10 carbon atoms, an alkoxy group having from 1 to 5 carbon atoms, phenyl group, or cyclohexyl group; B is selected from the group consisting of --CR 5 R 6 --, --S--, and --O--; R 5 and R 6 are each selected from the group consisting of a hydrogen atom, and an alkyl group having from 1 to 5 carbon atoms.",
    "15. A method as claimed in claim 1, wherein hydrogen is present in the reaction system.",
    "16. A method of producing alcohols which comprises: dimerizing a lower olefin in the presence of a catalyst comprising a nickel compound, an organic aluminum compound, and a phosphite compound having the general formula (I): ##STR33## wherein R 1, R 2, R 3, and R 4 are phenyl groups optionally substituted by substituents and may be different from each other, at least two of R 1, R 2, R 3, and R 4 have a hydrocarbon group as a substituent in the ortho position; A is a divalent aliphatic, alicyclic or aromatic hydrocarbon group which optionally has a substituent; and n is 0 or 1; to obtain dimerized olefins and, subjecting the dimerized olefins to a hydroformylation reaction and a hydrogenation reaction.",
    "17. A method as claimed in claim 16, wherein a rhodium catalyst is used in the hydroformylation reaction.",
    "18. A method as claimed in claim 16, wherein a cobalt catalyst is used in the hydroformylation reaction."
  ],
  "description_excerpt": "This invention relates to a method of dimerizing lower olefins such as ethylene, propylene, and butene using a specific catalyst and to a method of producing alcohols with the dimerized products.\n\nThe dimerized products of olefins produced through dimerization method according to the present invention may be hydroformylated by reaction with carbon monoxide and hydrogen in the presence of an VIII metal catalyst such as a rhodium catalyst. The resultant aldehydes may be hydrogenated to alcohols. Reaction of the said alcohols with carboxylic acids such as phthalic acid results in the formation of esters. These esters are of great industrial importance because of their application as plasticizers for synthetic resins.\n\nMany investigations have been made on catalytic systems that permit uniform dimerization of lower monoolefins such as ethylene, propylene, and butene. As the catalysts, Ziegler-type catalysts having transition metals as central catalyst component are usually superior in dimer selectivity of the lower monoolefins. In particular, satisfactory results have been obtained in dimerization activity and selectivity with a catalyst obtained from a mixture of a nickel compound and organic aluminum halide.\n\nInvestigations have also been made on catalytic systems containing organic phosphorus compounds as third additives to the above mentioned catalytic component. It is known that these additives affect on catalytic activity and product selectivity. As these catalytic system containing the organic phosphorus compounds, 1 Japanese Patent Publication No.",
  "cpc": [
    "C07C 29/16",
    "C07C 2/30",
    "C07C 2/34",
    "C07C 2531/02",
    "C07C 2531/04",
    "C07C 2531/14",
    "C07C 2531/16"
  ],
  "ipc": [
    "C07C 2/30",
    "C07C 2/34",
    "C07C 29/16"
  ],
  "assignees": [
    "Mitsubishi Kasei Corp"
  ],
  "inventors": [
    "Keiichi Sato",
    "Yuuji Kawaragi",
    "Yasuko Higashino"
  ],
  "filing_date": "1993-10-05",
  "publication_date": "1995-08-29",
  "grant_date": "1995-08-29",
  "priority_date": "1992-06-10",
  "application_number": "US-24421294-A",
  "family_id": "17446631",
  "cited_by_count": 42,
  "citations": [
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}