DE149346C - - Google Patents
Info
- Publication number
- DE149346C DE149346C DENDAT149346D DE149346DA DE149346C DE 149346 C DE149346 C DE 149346C DE NDAT149346 D DENDAT149346 D DE NDAT149346D DE 149346D A DE149346D A DE 149346DA DE 149346 C DE149346 C DE 149346C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- parts
- phenylglycine
- anthranilodiacetic
- carboxylic acid
- 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
- 239000002253 acid Substances 0.000 claims description 15
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 239000007800 oxidant agent Substances 0.000 claims description 3
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical compound CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 11
- PCKPVGOLPKLUHR-UHFFFAOYSA-N indoxyl Chemical group C1=CC=C2C(O)=CNC2=C1 PCKPVGOLPKLUHR-UHFFFAOYSA-N 0.000 description 10
- PJUXPMVQAZLJEX-UHFFFAOYSA-N 2-(carboxymethylamino)benzoic acid Chemical compound OC(=O)CNC1=CC=CC=C1C(O)=O PJUXPMVQAZLJEX-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- RRTQTOBOLIGMED-UHFFFAOYSA-N 2-(carboxyamino)-2-phenylacetic acid Chemical compound OC(=O)NC(C(O)=O)C1=CC=CC=C1 RRTQTOBOLIGMED-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- -1 phenylglycine carboxylic acid Chemical class 0.000 description 2
- KBQLZPUOEZHYAA-UHFFFAOYSA-N 2-[n-(carboxymethyl)-2-methylanilino]acetic acid Chemical compound CC1=CC=CC=C1N(CC(O)=O)CC(O)=O KBQLZPUOEZHYAA-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- ZGUNAGUHMKGQNY-ZETCQYMHSA-N L-alpha-phenylglycine zwitterion Chemical compound OC(=O)[C@@H](N)C1=CC=CC=C1 ZGUNAGUHMKGQNY-ZETCQYMHSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- ZGUNAGUHMKGQNY-UHFFFAOYSA-N alpha-phenylglycine Chemical compound OC(=O)C(N)C1=CC=CC=C1 ZGUNAGUHMKGQNY-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE149346C true DE149346C (enrdf_load_stackoverflow) |
Family
ID=416360
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT149346D Active DE149346C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE149346C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT149346D patent/DE149346C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE149346C (enrdf_load_stackoverflow) | ||
DE2709965A1 (de) | Verfahren zur farbverbesserung von ruebenschnitzeln | |
EP0163318B1 (de) | Neue 2-substituierte 3-Sulfopropyl-ammoniumbetaine und Verfahren zu ihrer Herstellung | |
DE945147C (de) | Verfahren zur Herstellung von Pyridin-2, 3-dicarbonsaeure | |
EP0149857A1 (de) | Verfahren zur Herstellung von Chinolinsäure aus Chinolin | |
DE286691C (enrdf_load_stackoverflow) | ||
DE664425C (de) | Verfahren zur Herstellung von Oxydationsprodukten hochmolekularer Amine | |
DE213593C (enrdf_load_stackoverflow) | ||
DE250154C (enrdf_load_stackoverflow) | ||
DE98939C (enrdf_load_stackoverflow) | ||
DE179295C (enrdf_load_stackoverflow) | ||
DE716960C (de) | Verfahren zur Herstellung von Oxalsaeure durch Oxydation von Lignin, Zellstoffablaugen oder aehnlichen Abfallerzeugnissen mit Salpetersaeure | |
DE283538C (enrdf_load_stackoverflow) | ||
DE238381C (enrdf_load_stackoverflow) | ||
DE93538C (enrdf_load_stackoverflow) | ||
DE117005C (enrdf_load_stackoverflow) | ||
DE199944C (enrdf_load_stackoverflow) | ||
DE574943C (de) | Verfahren zur Darstellung von Tetrazolen | |
DE526599C (de) | Verfahren zur Reinigung von stark salzsauren Holzzuckerloesungen | |
DE69035C (de) | Verfahren zur Darstellung von p-Aethoxyacetylamidochinolin. (4 | |
DE175295C (enrdf_load_stackoverflow) | ||
DE221849C (enrdf_load_stackoverflow) | ||
DE90206C (enrdf_load_stackoverflow) | ||
DE91503C (enrdf_load_stackoverflow) | ||
AT117475B (de) | Verfahren zur Darstellung von Substitutionsprodukten des ß-Jodpyridins. |