Production of 2-phenyl-3-nitrobutyric acid compounds
    1.
    发明授权
    Production of 2-phenyl-3-nitrobutyric acid compounds 失效
    2-苯基-3-硝基丁酸化合物的制备

    公开(公告)号:US3887617A

    公开(公告)日:1975-06-03

    申请号:US26643272

    申请日:1972-06-26

    Applicant: BASF AG

    CPC classification number: C07C201/12 C07C231/12 C07C205/53 C07C233/11

    Abstract: The production of compounds of 2-phenyl-3-nitrobutyric acid by reaction of 1-phenyl-2-nitroethenes with lithium carboxamides. The compounds which can be prepared according to the process of the invention are valuable starting materials for the production of dyes and pharmaceuticals.

    Abstract translation: 2-苯基-3-硝基丁酸的化合物通过1-苯基-2-硝基乙烯与氨基甲酰胺的反应生成。 可根据本发明方法制备的化合物是用于生产染料和药物的有价值的原料。

    2.
    发明专利
    未知

    公开(公告)号:DE59704125D1

    公开(公告)日:2001-09-13

    申请号:DE59704125

    申请日:1997-03-07

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP97/01163 Sec. 371 Date Sep. 18, 1997 Sec. 102(e) Date Sep. 18, 1998 PCT Filed Mar. 7, 1997 PCT Pub. No. WO97/34886 PCT Pub. Date Sep. 25, 1997Chiral compounds of the formula I where: R1,R2,R3,R4 are hydrogen or aromatic, aliphatic or araliphatic radicals having 1 to 40 carbon atoms, R5,R6,R7,R8 are aromatic or aliphatic radicals having 1 to 20 carbon atoms, with the proviso that at least one of the radicals R1 to R8 contains a polymerizable group, are used as dopes in liquid crystals, in compositions for coating substrates and in the preparation of interference pigments which can be used in printing inks and surface coatings.

    ELECTROPHILIC SUBSTITUTION OF NITROSAMINES

    公开(公告)号:CA1011750A

    公开(公告)日:1977-06-07

    申请号:CA168658

    申请日:1973-04-11

    Applicant: BASF AG

    Abstract: 1417338 Electrophilic substitution of nitrosamines BADISCHE ANILIN- & SODAFABRIK AG 13 April 1973 [15 April 1972 22 Sept 1972] 17818/73 Heading C2C Electrophilic substitution of a nitrosamine on the carbon atom α to the amino nitrogen is achieved by metallizing in the α position the nitrosamine of a secondary amine which bears at least one hydrogen atom in this position, and reacting the metallized product with an electrophite. In the nitrosamine R 1 R 2 N.NO, R 1 and R 2 may for example be alkyl, cyclohexyl, phenyl or benzyl, or the amino nitrogen may be part of a heterocyclic ring. The metallizing metal may be an alkali or alkaline earth metal or zinc, cadmium or monovalent copper, and organometallic compounds may be used as metallizing agent; lithium diisopropylamide is the preferred agent. Suitable electrophiles include carbonyl compounds, alkylating agents, e.g. alkyl or substituted alkyl halides, sulphates and sulphonates, acylating agent (carboxylic acid chlorides, esters, anhydrides, alkali metal salts, amides, nitriles, isocyanates, ketene and carbon dioxide); halohydrins obtained when using haloketones may react further by elimination of hydrogen halide to give epoxide; when using acyl halide, the resultant carbonyl compound may react with a further nitrosamine compound (e.g. PhCOCl with (CH 3 ) 2 N.NO gives PhCOR and/or PhC(OH)(R) 2 where R is CH 3 N(NO)CH 2 -). Inorganic electrophiles may also be used; use of iodine results in oxidative coupling of two nitrosamine molecules (e.g. RN(NO)CH 3 gives (RN(NO)CH 2 -) 2 where R is alkyl or aryl). Products may be reduced to hydrazines, or denitrosated to amines; products obtained when using carbonyl compounds contain hydroxy groups and may be dehydrated (e.g. benzaldehyde + dimethyl nitrosamine # PhCH(OH)- CH 2 N(NO)CH 3 # PhCH=CH-N(NO)CH 3 ).

    4.
    发明专利
    未知

    公开(公告)号:AT203529T

    公开(公告)日:2001-08-15

    申请号:AT97908197

    申请日:1997-03-07

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP97/01163 Sec. 371 Date Sep. 18, 1997 Sec. 102(e) Date Sep. 18, 1998 PCT Filed Mar. 7, 1997 PCT Pub. No. WO97/34886 PCT Pub. Date Sep. 25, 1997Chiral compounds of the formula I where: R1,R2,R3,R4 are hydrogen or aromatic, aliphatic or araliphatic radicals having 1 to 40 carbon atoms, R5,R6,R7,R8 are aromatic or aliphatic radicals having 1 to 20 carbon atoms, with the proviso that at least one of the radicals R1 to R8 contains a polymerizable group, are used as dopes in liquid crystals, in compositions for coating substrates and in the preparation of interference pigments which can be used in printing inks and surface coatings.

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