DE105199C - - Google Patents
Info
- Publication number
- DE105199C DE105199C DENDAT105199D DE105199DA DE105199C DE 105199 C DE105199 C DE 105199C DE NDAT105199 D DENDAT105199 D DE NDAT105199D DE 105199D A DE105199D A DE 105199DA DE 105199 C DE105199 C DE 105199C
- Authority
- DE
- Germany
- Prior art keywords
- acetanilide
- hydrochloric acid
- acid
- alcohol
- parts
- 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
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 claims description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 14
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 14
- 229960001413 acetanilide Drugs 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- -1 acetamidomethylchloracetophenone Chemical compound 0.000 claims description 2
- FXXACINHVKSMDR-UHFFFAOYSA-N acetyl bromide Chemical compound CC(Br)=O FXXACINHVKSMDR-UHFFFAOYSA-N 0.000 claims description 2
- 150000004982 aromatic amines Chemical class 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- FRXLFVNGTPQFEJ-UHFFFAOYSA-N 3-bromopropanoyl bromide Chemical compound BrCCC(Br)=O FRXLFVNGTPQFEJ-UHFFFAOYSA-N 0.000 claims 2
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 claims 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims 2
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 claims 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 claims 1
- QCXJEYYXVJIFCE-UHFFFAOYSA-N 4-acetamidobenzoic acid Chemical compound CC(=O)NC1=CC=C(C(O)=O)C=C1 QCXJEYYXVJIFCE-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000000155 melt Substances 0.000 claims 1
- KEBPJACCSMNODE-UHFFFAOYSA-N n-(1-chloro-2-oxo-2-phenylethyl)acetamide Chemical compound CC(=O)NC(Cl)C(=O)C1=CC=CC=C1 KEBPJACCSMNODE-UHFFFAOYSA-N 0.000 claims 1
- LLZKTKZPJBSEHD-UHFFFAOYSA-N n-[4-(2-bromopropanoyl)phenyl]acetamide Chemical compound CC(Br)C(=O)C1=CC=C(NC(C)=O)C=C1 LLZKTKZPJBSEHD-UHFFFAOYSA-N 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 238000007127 saponification reaction Methods 0.000 claims 1
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 6
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000008379 phenol ethers Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000004576 sand Substances 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 |
|---|---|
| DE105199C true DE105199C (en:Method) |
Family
ID=375507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT105199D Active DE105199C (en:Method) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE105199C (en:Method) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6814657B2 (en) | 2001-12-17 | 2004-11-09 | Hilti Aktiengesellschaft | Grinding wheel with grinding members |
-
0
- DE DENDAT105199D patent/DE105199C/de active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6814657B2 (en) | 2001-12-17 | 2004-11-09 | Hilti Aktiengesellschaft | Grinding wheel with grinding members |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE105199C (en:Method) | ||
| CH460041A (de) | Verfahren zur Herstellung von 4-substituierten 4'-tert.-Aminoalkoxyphenylen | |
| DE2513801A1 (de) | Neue fluorierte indazolderivate und verfahren zu ihrer herstellung | |
| DE3873983T2 (de) | Verfahren zur herstellung von halogenierten imiden. | |
| DE573722C (de) | Verfahren zur Darstellung von ª‡-Dicarbonylverbindungen | |
| DE574840C (de) | Verfahren zur Darstellung von Indolen | |
| DE280971C (en:Method) | ||
| DE920790C (de) | Verfahren zur Herstellung von Salicylsaeurearylamiden | |
| DE134979C (de) | Verfahren zur darstellung von benzylphtalimiden | |
| DE510435C (de) | Verfahren zur Darstellung von negativ substituierten Carbazolen | |
| DE2132961A1 (de) | Verfahren zur herstellung von n-alkylcarbazolen | |
| DE621710C (de) | Verfahren zur Darstellung von Chlor- und Bromverbindungen der p-Aminophenylalkylaether | |
| DE614195C (de) | Verfahren zur Darstellung von Dialkylaminocyclohexenonen | |
| DE843414C (de) | Verfahren zur Herstellung von 2-Aryl-3,4,6-triketo-2,3,4,5,6,7-hexahydro-pyrazolpyridinen | |
| DE888690C (de) | Verfahren zur Herstellung von Halogensubstitutionserzeugnissen aus ungesaettigten organischen Verbindungen | |
| DE591937C (de) | Verfahren zur Darstellung von Arsenverbindungen der Chinolinreihe | |
| DE85566C (en:Method) | ||
| DE866094C (de) | Verfahren zur Herstellung von organischen Verbindungen, vorzugsweise Polyaethinkoerpern, aus Aldehyd-Harzen | |
| DE607988C (de) | Verfahren zur Herstellung von 4-Oxycumaronen | |
| DE733965C (de) | Verfahren zur Herstellung von Kondensationsprodukten | |
| DE24317C (de) | Verfahren zur Darstellung der Oxyhydrochinaldine und der Methyl- und Aethyl-Derivate derselben | |
| DE97241C (en:Method) | ||
| DE1004189B (de) | Verfahren zur Herstellung von ª‰-Sulfamido-carbonsaeureamiden | |
| DE44238C (de) | Verfahren zur Darstellung von mono- und disubstituirten Dtalkylamidobenzoesäureamiden | |
| DE1768505A1 (de) | Phenaethylaminverbindungen und Verfahren zu ihrer Herstellung |