DE254091C - - Google Patents
Info
- 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.)
- Active
Links
- 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
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE254091C true DE254091C (cs) |
Family
ID=512308
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT254091D Active DE254091C (cs) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE254091C (cs) |
-
0
- DE DENDAT254091D patent/DE254091C/de active Active
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