4.
    发明专利
    未知

    公开(公告)号:DE59405805D1

    公开(公告)日:1998-05-28

    申请号:DE59405805

    申请日:1994-08-13

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP94/02708 Sec. 371 Date Feb. 15, 1996 Sec. 102(e) Date Feb. 15, 1996 PCT Filed Aug. 13, 1994 PCT Pub. No. WO95/06036 PCT Pub. Date Mar. 2, 1995A process for preparing pyrazole and its derivatives of the formula I I where R1, R2, R3 and R4 are each hydrogen, halogen, nitro, carboxyl, sulfonyl or C-organic radicals, from alpha,beta-unsaturated carbonyl compounds of the formula II II and hydrazine or hydrazine derivatives of the formula III H2N-NHR4 III wherein, initially without additional diluent, an alpha,beta-unsaturated carbonyl compound of the formula II is reacted with hydrazine or a hydrazine derivative of the formula III, and the resulting reaction mixture is reacted in another step with a mixture of sulfuric acid and iodine or a compound which liberates iodine or hydrogen iodide.

    5.
    发明专利
    未知

    公开(公告)号:BR8206023A

    公开(公告)日:1983-09-13

    申请号:BR8206023

    申请日:1982-10-15

    Applicant: BASF AG

    Abstract: 3-Isopropyl-2,1,3-benzothiadiazin-4-one-2,2-dioxide (bentazone) is isolated from waste water, originating from its preparation and working up, by treating the waste water with an acid to bring the pH initially to 7.5-9.5, adding 0.2-0.5% by volume, based on the waste water, of a 40-60 percent strength by weight aqueous bentazone salt solution and heating the mixture for 15-30 minutes at 75 DEG -110 DEG C. The solution thus treated is then cooled and brought to pH 1-3 with a mineral acid, whereupon the bentazone precipitates in a form which can be filtered off.

    9.
    发明专利
    未知

    公开(公告)号:FI68233B

    公开(公告)日:1985-04-30

    申请号:FI780694

    申请日:1978-03-01

    Applicant: BASF AG

    Abstract: New and valuable process for the manufacture of 2,1,3-thiadiazin-4-one-2,2-dioxide derivatives by reaction of anthranilic acid amide or aminopyridine carboxamide derivatives with sulfur trioxide derivatives to give the sulfamic acid salts, followed by cyclization of these salts.

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