PRODUCTION OF 2,4-DIMETHYLPYRROLE

    公开(公告)号:JP2000178250A

    公开(公告)日:2000-06-27

    申请号:JP35933999

    申请日:1999-12-17

    Applicant: BASF AG

    Abstract: PROBLEM TO BE SOLVED: To produce 2,4-dimethylpyrrole under much milder conditions of slighter aggressiveness thin well-known conditions according to a conventional technique. SOLUTION: A dicarboxylic acid alkyl ester which is a 2,4-dimethyl-3,5- bisalkoxycarbonylpyrrole is refluxed together with an aqueous solution of an alkali metal hydroxide at 10-30% concentration, advantageously a sodium hydroxide solution until a solid is converted into a solution and the reactional mixture is then neutralized with an acid and further refluxed until the decarbocylation is completed, i.e., the gas evolution is stopped.

    PRODUCTION OF SUBSTITUTED IMIDAZOLE

    公开(公告)号:JPH1087632A

    公开(公告)日:1998-04-07

    申请号:JP22248497

    申请日:1997-08-19

    Applicant: BASF AG

    Abstract: PROBLEM TO BE SOLVED: To obtain the subject compound useful as a precursor substance or an intermediate for producing dyestuffs, fiber auxiliaries, plastics, etc., by directly using an aqueous imidazole phase obtained on the synthesis of the substituted imidazole. SOLUTION: The aqueous phase of an imidazole compound of formula I (R , R , R are each H, a halogen, NO2 , etc.) is reacted with a compound of the formula: R -O-R (R is a 1-20C hydrocarbon; R is H or R ) in the presence of a catalyst such as the oxide of a metal belonging to the subgroup 4 in the main groups 2, 3, 4 in the periodic table, a phosphate salt, etc., at 220-550 deg.C to produce the substituted imidazole of formula II. The catalyst is used in the form of a fixed bed, and an advantageous catalyst comprises 40-99wt.% of SiO2 and 1-60wt.% of H3 PO4 , or comprises 70-90wt.% of Al2 O3 and 10-30wt.% of SiO2 . Water and the compound of formula I are used in amounts of 99.9-0.1wt.% and 0.1-99.9wt.%, especially advantageously 40-10wt.% and 60-90wt.%, respectively, in the reaction. The reaction temperature is 200-550 deg.C, especially advantageously 280-420 deg.C.

    PRODUCTION OF 2,4-DIMETHY-3,5-BISALKOXYCARBONYLLPYRROLE

    公开(公告)号:JP2000178251A

    公开(公告)日:2000-06-27

    申请号:JP35934099

    申请日:1999-12-17

    Applicant: BASF AG

    Abstract: PROBLEM TO BE SOLVED: To produce a 2,4-dimethyl-3,5-bisalkoxycarbonylpyrrole by enabling operations under milder conditions than those of a conventional technique and avoidance of the formation of by-products. SOLUTION: An alkyl acetoacetate is nitrosated to produce an alkyl 2- nitrosoacetoacetate, which is then reduced with hydrogen in the presence of a noble metal catalyst to form an amine. The resultant amino compound without isolation is condensed in the presence of the corresponding alkyl acetoacetate without undergoing the nitrosation to produce 2,4-dimethyl-3,5- bisalkoxycarbonylpyrrole.

    5.
    发明专利
    未知

    公开(公告)号:DE19803368A1

    公开(公告)日:1999-08-05

    申请号:DE19803368

    申请日:1998-01-29

    Applicant: BASF AG

    Abstract: Unsaturated cyclic ethers are produced from diols in high yield and with low hydrogenated byproduct formation, by use of a supported cobalt-noble metal catalyst that has been doped with sulfur. A process for the production of unsaturated cyclic ethers (I) of formula (1) comprises reaction of a diol (II) of formula: OH-CH(R )-Y-CH(R )-CH(R )-OH (2), in the liquid phase at 150-300 degrees C, in the presence of a supported cobalt- containing catalyst (III) that has not been activated by reduction prior to use. The cobalt containing catalyst (III) is impregnated with a noble metal consisting of platinum, palladium, rhodium, iridium, ruthenium, osmium and/or rhenium on an inert carrier that is doped with sulfur. Y = -(CHR )q- or -(CHR )q-O-; R - R = H or 1-4C alkyl; q = 0-3. An Independent claim is also included for the supported cobalt catalyst (III).

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