DE79857C - - Google Patents
Info
- Publication number
- DE79857C DE79857C DENDAT79857D DE79857DA DE79857C DE 79857 C DE79857 C DE 79857C DE NDAT79857 D DENDAT79857 D DE NDAT79857D DE 79857D A DE79857D A DE 79857DA DE 79857 C DE79857 C DE 79857C
- Authority
- DE
- Germany
- Prior art keywords
- amidophenol
- oxybenzylidene
- parts
- alkylated
- xxv
- 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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- 230000029936 alkylation Effects 0.000 claims description 2
- 238000005804 alkylation reaction Methods 0.000 claims description 2
- IJWFUEBTMMXDMR-UHFFFAOYSA-N chembl1903262 Chemical compound C1=CC(OCC)=CC=C1N=CC1=CC=CC=C1O IJWFUEBTMMXDMR-UHFFFAOYSA-N 0.000 claims 1
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IMPPGHMHELILKG-UHFFFAOYSA-N 4-ethoxyaniline Chemical compound CCOC1=CC=C(N)C=C1 IMPPGHMHELILKG-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- MUDBNSUKTFIAJT-UHFFFAOYSA-N Kerlin Natural products O1C2(C)CCC34COC(=O)C3=CCCC4C2(C)CC1C1=CC(=O)OC1 MUDBNSUKTFIAJT-UHFFFAOYSA-N 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 230000001754 anti-pyretic effect Effects 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 125000005998 bromoethyl group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical group [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
Landscapes
- Heat Sensitive Colour Forming Recording (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fireproofing Substances (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE79857C true DE79857C (enExample) |
Family
ID=352466
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT79857D Active DE79857C (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE79857C (enExample) |
-
0
- DE DENDAT79857D patent/DE79857C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE884500C (de) | Verfahren zur Herstellung von in 3-Stellung substituierten 4-Oxycumarinen | |
| DE79857C (enExample) | ||
| DE927092C (de) | Verfahren zur Herstellung von Thiophosphorsaeureestern | |
| DE838892C (de) | Verfahren zur Herstellung von diquarternaeren Ammoniumverbindungen | |
| DE667356C (de) | Verfahren zur Herstellung von Tetrahydro-p-oxazinoalkylarylketonen | |
| DE668741C (de) | Verfahren zur Darstellung von Jod und freie oder veraetherte Oxygruppen enthaltenden2-Phenylchinolin-4-carbonsaeuren | |
| DE837098C (de) | Verfahren zur Herstellung von quaternaeren 3-Oxyphenyl-ammoniumverbindungen | |
| DE682393C (de) | Verfahren zur Herstellung quaternaerer Stickstoffverbindungen | |
| DE1768399B2 (de) | O-Alkyl-O-aryl-thiolphosphorsäureester, Verfahren zu deren Herstellung und diese Verbindungen enthaltende insektizide und akarizide Mittel | |
| DE924450C (de) | Verfahren zur Herstellung von Cumarinderivaten | |
| DE1067822B (de) | Verfahren zur Herstellung neuer Hydantoine | |
| DE668387C (de) | Verfahren zur Herstellung von 1, 2, 3-substituierten 4-Acyl-5-pyrazolonen | |
| DE85566C (enExample) | ||
| DE127424C (enExample) | ||
| DE554553C (de) | Verfahren zur Darstellung von Phenylpropanolmethylamin | |
| DE406152C (de) | Verfahren zur Darstellung kuenstlicher Harze und OEle | |
| DE710768C (de) | Verfahren zur Herstellung von Phenolharzen | |
| DE1293779B (de) | Verfahren zur Herstellung von substituierten Tetrahydropyranen und 2, 3-Dihydropyranen | |
| DE816701C (de) | Verfahren zur Herstellung phosphorhaltiger Abkoemmlinge des m-Dimethylaminophenols | |
| DE164366C (enExample) | ||
| DE209609C (enExample) | ||
| DE630910C (de) | Verfahren zur Herstellung von C, C-disubstituierten Barbitursaeuren | |
| DE279389C (enExample) | ||
| DE884497C (de) | Verfahren zur Herstellung von 2, 3-Di-(p-oxyphenyl)-butadien-verbindungen oder derenHomologen | |
| DE434728C (de) | Verfahren zur Herstellung halogenierter Alkohole |