DE92796C - - Google Patents
Info
- Publication number
- DE92796C DE92796C DENDAT92796D DE92796DA DE92796C DE 92796 C DE92796 C DE 92796C DE NDAT92796 D DENDAT92796 D DE NDAT92796D DE 92796D A DE92796D A DE 92796DA DE 92796 C DE92796 C DE 92796C
- Authority
- DE
- Germany
- Prior art keywords
- sodium
- acid
- alcohol
- impure
- acetic 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000011734 sodium Substances 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- HVBSAKJJOYLTQU-UHFFFAOYSA-N Sulfanilic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 claims description 5
- 229950000244 sulfanilic acid Drugs 0.000 claims description 5
- 229960000583 Acetic Acid Drugs 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- BDKZHNJTLHOSDW-UHFFFAOYSA-N [Na].CC(O)=O Chemical compound [Na].CC(O)=O BDKZHNJTLHOSDW-UHFFFAOYSA-N 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 3
- 239000012362 glacial acetic acid Substances 0.000 claims description 3
- IGWIEYXEWVUGCK-UHFFFAOYSA-N 4-aminobenzenesulfonic acid;sodium Chemical compound [Na].NC1=CC=C(S(O)(=O)=O)C=C1 IGWIEYXEWVUGCK-UHFFFAOYSA-N 0.000 claims 1
- 238000006640 acetylation reaction Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 2
- FZERHIULMFGESH-UHFFFAOYSA-N Acetanilide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K Iron(III) chloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N Sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 230000001754 anti-pyretic Effects 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- TUCNEACPLKLKNU-UHFFFAOYSA-N ethanone Chemical compound C[C]=O TUCNEACPLKLKNU-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- KSVSZLXDULFGDQ-UHFFFAOYSA-M sodium;4-aminobenzenesulfonate Chemical compound [Na+].NC1=CC=C(S([O-])(=O)=O)C=C1 KSVSZLXDULFGDQ-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE92796C true DE92796C (ja) |
Family
ID=364278
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT92796D Active DE92796C (ja) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE92796C (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0095177A1 (de) * | 1982-05-26 | 1983-11-30 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von N-Acetylaminoarylsulfonsäuren |
-
0
- DE DENDAT92796D patent/DE92796C/de active Active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0095177A1 (de) * | 1982-05-26 | 1983-11-30 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von N-Acetylaminoarylsulfonsäuren |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE92796C (ja) | ||
DE927140C (de) | Verfahren zur Fraktionierung von Staerke | |
DE874915C (de) | Verfahren zur Herstellung von normalem Bleisalicylat | |
AT200154B (de) | Verfahren zur Herstellung von Citrullin | |
DE125988C (ja) | ||
DE68719C (de) | Verfahren zur Darstellung von p-Aethoxyphenylhydrazin und p-Aethoxyhydracetin | |
DE562897C (de) | Verfahren zur Herstellung von Derivaten der Benzol-, Naphthalin- und Acenaphthenreihen | |
DE567524C (de) | Verfahren zur Darstellung von Azofarbstoffen | |
DE733809C (de) | Verfahren zur Gewinnung von Glykosiden aus Strophanthus Kombe | |
DE515468C (de) | Verfahren zur Darstellung von ª‰-Naphthylaminophenoxyfettsaeuren | |
DE651613C (de) | Verfahren zur Herstellung von optisch aktivem trans-ªð-Oxycampher | |
DE44248C (ja) | ||
DE853288C (de) | Verfahren zur Herstellung wasserloeslicher, hochbasischer Aluminiumverbindungen | |
DE708939C (de) | Verfahren zur Herstellung gonadotroper Hormone aus waessrigen Ausgangsloesungen | |
DE619348C (de) | Verfahren zur Herstellung von reinem Diacetyl aus Holzessig oder anderen Diacetyl enthaltenden Gemischen | |
DE244320C (ja) | ||
DE872206C (de) | Verfahren zur Herstellung von Methylchlorphenoxyfettsaeuren | |
DE854524C (de) | Verfahren zur Herstellung von Chloraryloxyfettsaeuren | |
DE948158C (de) | Verfahren zur Herstellung von Zink-Komplexsalzen von Tripeptiden | |
DE579820C (de) | Verfahren zur Gewinnung weiblicher Sexualhormone in kristallisierter Form | |
DE654559C (de) | Verfahren zur Herstellung von Naphthalindicarbonsaeurederivaten | |
DE171991C (ja) | ||
DE766094C (de) | Verfahren zur Gewinnung von 2, 4-Dimethylchinolin aus Steinkohlenteer | |
DE1543521C (de) | Verfahren zur Herstellung von jodiertem Lecithin | |
AT101671B (de) | Verfahren zur Darstellung von Karbonsäureestern mehrwertiger, halogenierter Alkohole. |