DE113720C - - Google Patents
Info
- Publication number
- DE113720C DE113720C DENDAT113720D DE113720DA DE113720C DE 113720 C DE113720 C DE 113720C DE NDAT113720 D DENDAT113720 D DE NDAT113720D DE 113720D A DE113720D A DE 113720DA DE 113720 C DE113720 C DE 113720C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- saccharin
- sulfamidobenzoic
- sulfuric acid
- temperature
- 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
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 claims description 13
- 229940081974 saccharin Drugs 0.000 claims description 12
- 235000019204 saccharin Nutrition 0.000 claims description 12
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 claims description 12
- KDNIOKSLVIGAAN-UHFFFAOYSA-N 2-sulfamoylbenzoic acid Chemical compound NS(=O)(=O)C1=CC=CC=C1C(O)=O KDNIOKSLVIGAAN-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 claims description 4
- FWFGVMYFCODZRD-UHFFFAOYSA-N oxidanium;hydrogen sulfate Chemical compound O.OS(O)(=O)=O FWFGVMYFCODZRD-UHFFFAOYSA-N 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
- C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE113720C true DE113720C (enrdf_load_stackoverflow) |
Family
ID=383282
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT113720D Active DE113720C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE113720C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT113720D patent/DE113720C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2601681A1 (de) | Verfahren zur herstellung von 4,4'- isopropyliden-bis(2,6-dibromphenol) | |
DE113720C (enrdf_load_stackoverflow) | ||
EP0021211B1 (de) | Verfahren zur Herstellung von Dimethylcarbonat | |
DE2738643C2 (de) | Verfahren zur Herstellung von α-Cyano-3-phenoxy-benzylalkohol | |
DE60314769T2 (de) | Reinigungsverfahren von 1,4-butanediol mononitrat | |
EP0050290A1 (de) | Verfahren zur Herstellung von Alkalisalzen der Imidodisulfonsäure | |
DE3921131A1 (de) | Verfahren zur herstellung von hellfarbigen niederen alkansulfonsaeuren, insbesondere methansulfonsaeure | |
DE2503504B1 (de) | Verfahren zur herstellung von kernjodierten jodverbindungen mit aromatischem charakter | |
EP0077537B1 (de) | Verfahren zur Herstellung von 6-Chlor-3-toluidin-4-sulfonsäure | |
DE1276635B (de) | Verfahren zur Herstellung von Kaliumsorbat | |
EP0014680B1 (de) | Verfahren zur Herstellung des Magnesiumsalzes von 3-Nitronaphthalin-1,5-disulfonsäure (Nitro-Armstrong-Säure) | |
DE611397C (de) | Verfahren zur Darstellung von wasserloeslichen Zinkverbindungen der Oxymethansulfinsaeure | |
DE1215173B (de) | Verfahren zur Herstellung von kristallinem Natriumsalicylat | |
DE2127898C3 (de) | Verfahren zur Herstellung von ge gebenenfalls inert substituierten o und p Aminothiophenolen | |
EP0475226B1 (de) | Verfahren zur Herstellung von 2-Mercapto-benzothiazol | |
DE2535337C2 (de) | Verfahren zur Herstellung von 1-Amino-naphthalin-7-sulfonsäure | |
DE819692C (de) | Verfahren zur Herstellung von 4-Amino-2, 6-dialkyl- bzw. -diaralkylpyrimidinen | |
DE591889C (de) | Verfahren zur Herstellung von Benzoesaeure und benzoesauren Salzen | |
EP0216204B1 (de) | Verfahren zur Herstellung von 1,3,6,8-Tetrabrompyren | |
DE202825C (enrdf_load_stackoverflow) | ||
DE117539C (enrdf_load_stackoverflow) | ||
DE152652C (enrdf_load_stackoverflow) | ||
DE942091C (de) | Verfahren zur Herstellung von Ammoniumsulfat, insbesondere fuer Duengezwecke | |
DE2651418A1 (de) | Verfahren zur aufarbeitung der bei der herstellung von natriumdithionit nach dem natriumformiatverfahren anfallenden mutterlaugen | |
DE1792010A1 (de) | Verfahren zur Herstellung von Mono- und/oder Diammoniumphosphat aus natuerlichen Phosphaten |