DE96851C - - Google Patents
Info
- Publication number
- DE96851C DE96851C DENDAT96851D DE96851DA DE96851C DE 96851 C DE96851 C DE 96851C DE NDAT96851 D DENDAT96851 D DE NDAT96851D DE 96851D A DE96851D A DE 96851DA DE 96851 C DE96851 C DE 96851C
- Authority
- DE
- Germany
- Prior art keywords
- formaldehyde
- alcohol
- aniline
- amidobenzyl
- toluidine
- 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
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 25
- 239000002253 acid Substances 0.000 claims description 8
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 150000007513 acids Chemical class 0.000 claims description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
- 239000011707 mineral Substances 0.000 claims description 4
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- SQGYOTSLMSWVJD-UHFFFAOYSA-N Silver nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- -1 acids Amido alcohols Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- MMCPOSDMTGQNKG-UHFFFAOYSA-N Anilinium chloride Chemical compound Cl.NC1=CC=CC=C1 MMCPOSDMTGQNKG-UHFFFAOYSA-N 0.000 description 1
- 210000004940 Nucleus Anatomy 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000005591 charge neutralization Effects 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- OGVXWEOZQMAAIM-UHFFFAOYSA-N hydron;2-methylaniline;chloride Chemical compound Cl.CC1=CC=CC=C1N OGVXWEOZQMAAIM-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000001264 neutralization Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE96851C true DE96851C (nl) |
Family
ID=367949
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT96851D Active DE96851C (nl) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE96851C (nl) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3095446A (en) * | 1959-05-12 | 1963-06-25 | Ciba Geigy Corp | Haloalkylaniline disulfonyl chlorides |
-
0
- DE DENDAT96851D patent/DE96851C/de active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3095446A (en) * | 1959-05-12 | 1963-06-25 | Ciba Geigy Corp | Haloalkylaniline disulfonyl chlorides |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH669593A5 (nl) | ||
| DE3025094A1 (de) | Vernetzte cellulosesulfatester, deren herstellung und verwendung | |
| DE96851C (nl) | ||
| DE1518289A1 (de) | Neue quaternaere Ammoniumsalze mit desinfizierender Wirkung und Verfahren zur Herstellung derselben | |
| DE2703919C2 (de) | Verfahren zur Herstellung von p-Nitroso-diphenylhydroxylaminen | |
| DE762425C (de) | Verfahren zur Herstellung von eine acylierte Benzylaminogruppe enthaltenden quartaeren Ammoniumverbindungen | |
| DE715541C (de) | Verfahren zur Herstellung von halogenwasserstoffsauren Salzen substituierter Isothioharnstoffe | |
| DE99542C (nl) | ||
| DE97710C (nl) | ||
| DE1518608C3 (de) | Verfahren zur Herstellung von N-PhenyW-alkoxy-NP-alkyl-harnstoffen | |
| DE889694C (de) | Verfahren zur Herstellung von Polystyrol-Derivaten | |
| DE206456C (nl) | ||
| DE155628C (nl) | ||
| DE112175C (nl) | ||
| DE415318C (de) | Verfahren zur Herstellung von 4-Arylamino-1-arylimino-2-naphthochinonen | |
| DE519449C (de) | Verfahren zur Herstellung von N: N-Thioderivaten von Aminen | |
| AT226677B (de) | Verfahren zur Herstellung von Bromderivaten organischer Verbindungen mit mindestens 2 nicht-kondensierten Benzolkernen, insbesondere des Diphenyls, des Diphenyläthers oder deren Homologe, die 4 und mehr Bromatome im Molekül enthalten | |
| AT152838B (de) | Verfahren zur Darstellung von Pyridinderivaten. | |
| DE1273529B (de) | Verfahren zur Herstellung von Diorganozinn-S, O-mercapto-acylaten | |
| DD240200A1 (de) | Verfahren zur herstellung von 4,4'-dinitrostilben-2,2'-disulfonsaeure i | |
| DE268451C (nl) | ||
| DE179946C (nl) | ||
| DE1470240C (de) | Adrenochrom monoguanylhydrazon und seine Salze mit anorganischen Sauren, Car bonsauren und Sulfonsäuren und Verfahren zu deren Herstellung | |
| DE121683C (nl) | ||
| DE513205C (de) | Verfahren zur Herstellung von Derivaten der Aminoarylantimonverbindungen |