DE341112C - - Google Patents
Info
- Publication number
- DE341112C DE341112C DENDAT341112D DE341112DA DE341112C DE 341112 C DE341112 C DE 341112C DE NDAT341112 D DENDAT341112 D DE NDAT341112D DE 341112D A DE341112D A DE 341112DA DE 341112 C DE341112 C DE 341112C
- Authority
- DE
- Germany
- Prior art keywords
- diarylamines
- aryl
- substituted
- derivatives
- hydrochloric 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
- -1 aluminum halides Chemical class 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- 125000005266 diarylamine group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- UWCPWBIMRYXUOU-UHFFFAOYSA-N 1-phenylindole-2,3-dione Chemical compound C12=CC=CC=C2C(=O)C(=O)N1C1=CC=CC=C1 UWCPWBIMRYXUOU-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 150000005623 oxindoles Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- PVFOMCVHYWHZJE-UHFFFAOYSA-N trichloroacetyl chloride Chemical compound ClC(=O)C(Cl)(Cl)Cl PVFOMCVHYWHZJE-UHFFFAOYSA-N 0.000 description 2
- JQVZXTCBSIOSRL-UHFFFAOYSA-N 2,2,2-trichloro-n,n-diphenylacetamide Chemical compound C=1C=CC=CC=1N(C(=O)C(Cl)(Cl)Cl)C1=CC=CC=C1 JQVZXTCBSIOSRL-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE341112C true DE341112C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Family
ID=571599
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT341112D Active DE341112C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE341112C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
-
0
- DE DENDAT341112D patent/DE341112C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1695753A1 (de) | Verbesserungen in der Herstellung von 4-Oxopiperidinverbindungen und gewisser neuer 4-Oxopiperidinverbindungen | |
| DE1167328B (de) | Verfahren zur Herstellung von Salicylsaeureaniliden | |
| DE1052984B (de) | Verfahren zur Herstellung neuer organischer Phosphorverbindungen | |
| DE1266766B (de) | Verfahren zur Herstellung von p-Aminodiphenylamin | |
| DE341112C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE1816993B2 (de) | Verfahren zur herstellung von indolyl-3-essigsaeuren | |
| DE964050C (de) | Verfahren zur Herstellung von Thiophenylpyridylaminen | |
| DE1906087A1 (de) | Oxodihydrobenzoxazinderivate und Verfahren zu ihrer Herstellung | |
| DE703899C (de) | Verfahren zum Dehydrieren von Imidazolinen | |
| DE960813C (de) | Verfahren zur Herstellung von ungesaettigten ª†- und ª€-Laktonen | |
| DE1545672A1 (de) | Dikarbonsaeureimidderivate und Verfahren zu ihrer Herstellung | |
| DE951995C (de) | Verfahren zur Herstellung von 1, 4-Dihydrazino-o-diazinen | |
| DE749643C (de) | Verfahren zur Herstellung ungesaettigter Carbonsaeureamide | |
| DE531083C (de) | Verfahren zur Darstellung von 5,6-Dialkoxy-8-aminochinolinen | |
| DE277396C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE610306C (de) | Verfahren zur Darstellung von gemischten Anhydriden zwischen Borsaeure und organischen Saeuren | |
| DE1643686C3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| AT262995B (de) | Verfahren zur Herstellung von neuen 2-Oxo-tetrahydro-imidazolderivaten | |
| DE546827C (de) | Verfahren zur Herstellung von Monooxaminsaeuren des 4íñ4'-Diaminodiphenyl-1íñ1'-cyklohexans und seiner Substitutionsprodukte | |
| DE893949C (de) | Verfahren zur Herstellung von aliphatischen Harnstoffderivaten | |
| DE939479C (de) | Sparbeizmittel und Verfahren zu ihrer Herstellung | |
| DE911259C (de) | Verfahren zur Herstellung von O-Phenylderivaten der Oxybenzal-thiosemicarbazone | |
| DE736024C (de) | Verfahren zur Herstellung sauerstoffhaltiger Anthracenabkoemmlinge | |
| DE69930C (de) | Verfahren zur Darstellung von p-Methoxyphenyldimethylpyrazolon | |
| DE1277862B (de) | Verfahren zur Herstellung von Dicarvocrotid und Tricarvocrotid |