Production of 3-nitro-p-cresol-(1)
    1.
    发明授权
    Production of 3-nitro-p-cresol-(1) 失效
    生产3-硝基对甲酚(1)

    公开(公告)号:US3911031A

    公开(公告)日:1975-10-07

    申请号:US34134873

    申请日:1973-03-15

    Applicant: BASF AG

    CPC classification number: C07C201/08 C07C205/22

    Abstract: 3-NITRO-P-CRESOL-(1) IS PRODUCED BY NITRATION OF P-CRESOL CARBONATE, PRECIPITATION OF 3-NITRO-P-CRESOL CARBONATE BY DILUTION WITH WATER AT 85* TO 100*C and saponification of the carbonate in aqueous ammonia at 60* to 80*C or in the presence of amines at a temperature of not more than 80*C. The product is a starting material for the production of dyes and herbicides.

    Abstract translation: 3-NITRO-P-CRESOL-(1)由碳酸亚铁制成,通过在85℃至100℃下用水稀释并将其在氨水中皂化,得到3-硝基 - 碳酸甲酯, 在60℃至80℃下或在不高于80℃的温度下在胺存在下进行。该产物是用于生产染料和除草剂的原料。

    3.
    发明专利
    未知

    公开(公告)号:DE59005479D1

    公开(公告)日:1994-05-26

    申请号:DE59005479

    申请日:1990-11-28

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP90/02036 Sec. 371 Date Feb. 27, 1992 Sec. 102(e) Date Feb. 27, 1992 PCT Filed Nov. 28, 1990 PCT Pub. No. WO91/08264 PCT Pub. Date Jun. 13, 1991.Quinophthalone derivatives of the formula I I where the group A completes substituted or unsubstituted heteroaromatic rings and the group B completes a substituted or unsubstituted aromatic ring, are prepared by reacting a methyl-substituted heterocyclic compound of the formula II II with an anhydride of an aromatic dicarboxylic acid of the formula III III or the corresponding free dicarboxylic acid (IIIa) in the presence of an acid and of an organic solvent, the organic solvent used being an alkyl benzoate.

    MANUFACTURE OF A RED PIGMENT FROM PERYLENE-3,4,9,10-TETRACARBOXYLIC ACID N,N'-BISMETHYLIMIDE

    公开(公告)号:GB2000168B

    公开(公告)日:1982-01-27

    申请号:GB7827074

    申请日:1978-06-16

    Applicant: BASF AG

    Abstract: A process for the manufacture of a red pigment from perylene-3,4,9,10-tetracarboxylic acid N,N'-bis-methylimide which has been obtained by methylating the corresponding diimide or by fusing naphthalic acid N-methylimide with an alkali metal hydroxide which comprises vatting a suspension of N,N'-bis-methylimide dye with 0.5-1.5 times by weight of an alkali metal dithionite in the presence of up to 4 times by weight of an alkali metal hydroxide relative to the quantity of the dithionite, at a temperature of from room temperature to 100 DEG C., to obtain the corresponding leuco compound, cooling the resulting solution to 20 DEG -40 DEG C., isolating and washing the leuco compound with fresh vatting solution until the solution is virtually colorless and clean and then oxidizing the leuco compound.

    5.
    发明专利
    未知

    公开(公告)号:DE59006992D1

    公开(公告)日:1994-10-06

    申请号:DE59006992

    申请日:1990-06-27

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP90/01030 Sec. 371 Date Oct. 22, 1991 Sec. 102(e) Date Oct. 22, 1991 PCT Filed Jun. 27, 1990 PCT Pub. No. WO91/00317 PCT Pub. Date Jan. 10, 1991.Anthraquinone dyes I I (Ar = aryl, A = anthraquinonyl) are prepared by reacting a aryldihalotriazine II II (Hal = chlorine or bromine) with an aminoanthraquinone III A-NH2 in an N-C1-C4 -alkylpyrrolid-2-one or -piperid-2-one, N-di-C1-C4 -alkylacetamide or -propionamide or urea derivatives of the formula IV IV (R = identical or different alkyl groups of from 1 to 4 carbon atoms which can also be linked together to form a 5- or 6-membered ring containing the urea group) as solvent.

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