DE254091C - - Google Patents

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Publication number

DE254091C

DE254091C DENDAT254091D DE254091DA DE254091C DE 254091 C DE254091 C DE 254091C DE NDAT254091 D DENDAT254091 D DE NDAT254091D DE 254091D A DE254091D A DE 254091DA DE 254091 C DE254091 C DE 254091C

Authority

DE

Germany

Prior art keywords

acid

parts

acids

derivatives

aminobenzoylbenzoic

Prior art date

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

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• GLPFSDPAITZWBL-UHFFFAOYSA-N 2-(3-aminobenzoyl)benzoic acid Chemical class NC1=CC=CC(C(=O)C=2C(=CC=CC=2)C(O)=O)=C1 GLPFSDPAITZWBL-UHFFFAOYSA-N 0.000 claims description 4
• 239000002253 acid Substances 0.000 claims description 4
• 229910052736 halogen Inorganic materials 0.000 claims description 4
• 239000003795 chemical substances by application Substances 0.000 claims description 3
• 150000002367 halogens Chemical class 0.000 claims description 3
• 238000000034 method Methods 0.000 claims description 3
• 150000007513 acids Chemical class 0.000 claims description 2
• 238000002360 preparation method Methods 0.000 claims description 2
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
• WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic acid anhydride Natural products CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 7
• 229960000583 acetic acid Drugs 0.000 description 4
• 238000002844 melting Methods 0.000 description 4
• 230000008018 melting Effects 0.000 description 4
• 239000012362 glacial acetic acid Substances 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
• PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
• 150000004056 anthraquinones Chemical class 0.000 description 2
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
• 229910052794 bromium Inorganic materials 0.000 description 2
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• WLJOSECGCGIVLK-UHFFFAOYSA-N 2-(3-amino-4-methylbenzoyl)benzoic acid Chemical compound C1=C(N)C(C)=CC=C1C(=O)C1=CC=CC=C1C(O)=O WLJOSECGCGIVLK-UHFFFAOYSA-N 0.000 description 1
• RWHRIIMYBNGFEV-UHFFFAOYSA-N 2-(4-carboxybenzoyl)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(=O)C1=CC=CC=C1C(O)=O RWHRIIMYBNGFEV-UHFFFAOYSA-N 0.000 description 1
• CFIUKBMYLCDCAW-UHFFFAOYSA-N 2-(5-acetamido-2-bromo-4-methylbenzoyl)benzoic acid Chemical compound BrC1=C(C(=O)C2=C(C(=O)O)C=CC=C2)C=C(C(=C1)C)NC(C)=O CFIUKBMYLCDCAW-UHFFFAOYSA-N 0.000 description 1
• NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical class CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
• CEFCGEAGZQDGOY-UHFFFAOYSA-N 2-acetamido-5-bromo-4-(2-carboxybenzoyl)benzoic acid Chemical compound BrC1=C(C(=O)C2=C(C(=O)O)C=CC=C2)C=C(C(=C1)C(=O)O)NC(C)=O CEFCGEAGZQDGOY-UHFFFAOYSA-N 0.000 description 1
• ALCCIWCIVXRVCD-UHFFFAOYSA-N 2-benzoyl-3-methylbenzoic acid Chemical compound CC1=CC=CC(C(O)=O)=C1C(=O)C1=CC=CC=C1 ALCCIWCIVXRVCD-UHFFFAOYSA-N 0.000 description 1
• FGTYTUFKXYPTML-UHFFFAOYSA-N 2-benzoylbenzoic acid Chemical class OC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 FGTYTUFKXYPTML-UHFFFAOYSA-N 0.000 description 1
• YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 1
• 239000005711 Benzoic acid Substances 0.000 description 1
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
• 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
• 238000005267 amalgamation Methods 0.000 description 1
• -1 amino-4-methylbenzoylbenzoic acid Chemical compound 0.000 description 1
• 229910052801 chlorine Inorganic materials 0.000 description 1
• 239000000460 chlorine Substances 0.000 description 1
• 125000001309 chloro group Chemical group Cl* 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• 230000026030 halogenation Effects 0.000 description 1
• 238000005658 halogenation reaction Methods 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 239000007858 starting material Substances 0.000 description 1
• 238000010792 warming Methods 0.000 description 1