DE220839C - - Google Patents
Info
- Publication number
- DE220839C DE220839C DENDAT220839D DE220839DA DE220839C DE 220839 C DE220839 C DE 220839C DE NDAT220839 D DENDAT220839 D DE NDAT220839D DE 220839D A DE220839D A DE 220839DA DE 220839 C DE220839 C DE 220839C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- formaldehyde
- parts
- needles
- halogen
- 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
- -1 halogen derivatives of anthranilic acid Formaldehyde Chemical class 0.000 claims description 12
- LELOWRISYMNNSU-UHFFFAOYSA-N Hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 150000002825 nitriles Chemical class 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- 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 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000006467 substitution reaction Methods 0.000 claims description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 16
- 239000002253 acid Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- RWZYAGGXGHYGMB-UHFFFAOYSA-N Anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 5
- CJKYKXAESHUOOV-UHFFFAOYSA-N 2-amino-3,4,5,6-tetrachlorobenzoic acid Chemical compound NC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(O)=O CJKYKXAESHUOOV-UHFFFAOYSA-N 0.000 description 4
- NNFCIKHAZHQZJG-UHFFFAOYSA-N Potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 229960000583 Acetic Acid Drugs 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- 150000002367 halogens Chemical group 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- JWQKYNJEPDPTQG-UHFFFAOYSA-N 2-(dichloroamino)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1N(Cl)Cl JWQKYNJEPDPTQG-UHFFFAOYSA-N 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N Hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating Effects 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- CCJWAFRVAHAVKQ-UHFFFAOYSA-N 2-(dibromoamino)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1N(Br)Br CCJWAFRVAHAVKQ-UHFFFAOYSA-N 0.000 description 1
- PLAZTCDQAHEYBI-UHFFFAOYSA-N 2-Nitrotoluene Chemical compound CC1=CC=CC=C1[N+]([O-])=O PLAZTCDQAHEYBI-UHFFFAOYSA-N 0.000 description 1
- VLHPTNVVTJTDHN-UHFFFAOYSA-N 2-carbamoyl-3,4,5,6-tetrachlorobenzoic acid Chemical compound NC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(O)=O VLHPTNVVTJTDHN-UHFFFAOYSA-N 0.000 description 1
- WZHHYIOUKQNLQM-UHFFFAOYSA-N 3,4,5,6-tetrachlorophthalic acid Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(O)=O WZHHYIOUKQNLQM-UHFFFAOYSA-N 0.000 description 1
- 229940097275 Indigo Drugs 0.000 description 1
- 240000007871 Indigofera tinctoria Species 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium(0) Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- AUHHYELHRWCWEZ-UHFFFAOYSA-N tetrachlorophthalic anhydride Chemical compound ClC1=C(Cl)C(Cl)=C2C(=O)OC(=O)C2=C1Cl AUHHYELHRWCWEZ-UHFFFAOYSA-N 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE220839C true DE220839C (ja) |
Family
ID=481861
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT220839D Active DE220839C (ja) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE220839C (ja) |
-
0
- DE DENDAT220839D patent/DE220839C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE220839C (ja) | ||
DE845940C (de) | Verfahren zur Herstellung von Derivaten des Pyrimidinopyrimidins | |
DE282711C (ja) | ||
DE86150C (de) | Verfahren zur einführung von aminresten in oxyanthrachinone | |
DE3511545A1 (de) | 4,4'-diaminodiphenylverbindungen, verfahren zu ihrer herstellung und ihre verwendung | |
DE145062C (ja) | ||
DE276331C (ja) | ||
DE870553C (de) | Verfahren zur Herstellung von Thiosemicarbazonen | |
DE727697C (de) | Verfahren zur Herstellung von Derivaten schwer- bis unloeslicher, mindestens eine Hydroxylgruppe enthaltender Azofarbstoffe | |
DE216749C (ja) | ||
DE148179C (ja) | ||
DE859314C (de) | Verfahren zur Herstellung von Dipropionsaeuren der heterocyclischen Reihe | |
DE46438C (de) | Verfahren zur Darstellung von Tetrazofarbstoffen aus Carbazo) | |
DE97673C (ja) | ||
DE44238C (de) | Verfahren zur Darstellung von mono- und disubstituirten Dtalkylamidobenzoesäureamiden | |
DE360425C (de) | Verfahren zur Darstellung einheitlicher Arylthioglykolsaeuren | |
DE216748C (ja) | ||
DE484664C (de) | Verfahren zur Darstellung von Sulfoderivaten der Oxyarylcarbonsaeurearylide | |
DE236046C (ja) | ||
DE73369C (de) | Verfahren zur Darstellung von Azofarbstoffen mit m-Phenylendiamindisulfosäure | |
DE210886C (ja) | ||
DE76491C (de) | Verfahren zur Darstellung von Amidotriazinen aus Chrysoi'dinen durch Aldehyde | |
DE58614C (de) | Verfahren zur Darstellung einer Amidonaphtoxylessigsäure und einer Sulfosäure derselben | |
DE53436C (de) | Verfahren zur Darstellung von Diamidophenyltolylsulfon und dessen Mono- und DisuKosäuTe. {1. ZAvsatx x\w» Pat-evAe. Nr. 33088.) | |
DE1795797C3 (de) | Verfahren zur Herstellung von 3-Nitro-pyridinderivaten |