DE170630C - - Google Patents
Info
- Publication number
- DE170630C DE170630C DENDAT170630D DE170630DA DE170630C DE 170630 C DE170630 C DE 170630C DE NDAT170630 D DENDAT170630 D DE NDAT170630D DE 170630D A DE170630D A DE 170630DA DE 170630 C DE170630 C DE 170630C
- Authority
- DE
- Germany
- Prior art keywords
- naphthylamine
- sulfonic acid
- solution
- hydrochloric acid
- heated
- 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
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 150000004982 aromatic amines Chemical class 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- -1 naphthylamine sulfonic acids Chemical class 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000005002 naphthylamines Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/47—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton having at least one of the sulfo groups bound to a carbon atom of a six-membered aromatic ring being part of a condensed ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE170630C true DE170630C (enrdf_load_stackoverflow) |
Family
ID=435660
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT170630D Active DE170630C (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE170630C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT170630D patent/DE170630C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE170630C (enrdf_load_stackoverflow) | ||
| DE2424372C3 (de) | Verfahren zur Herstellung von Isonitrosoacetaniliden | |
| DE447015C (de) | Verfahren zur Darstellung von Farbstoffen | |
| DE572204C (de) | Verfahren zur Herstellung von Aminoaethansulfonsaeuren | |
| DE470503C (de) | Verfahren zur Darstellung von Anthrachinonderivaten | |
| DE866647C (de) | Verfahren zur Herstellung von sekundaeren 1, 3-Alkendiaminen | |
| DE586806C (de) | Verfahren zur Darstellung von symmetrischen Di-(arylamino)-oxybenzolen | |
| DE638374C (de) | Verfahren zur Herstellung einer hydroaromatischen Oxycarbonsaeure | |
| DE2541663A1 (de) | Verfahren zur herstellung von aminoanthrachinonen | |
| DE586647C (de) | Verfahren zur Darstellung von symmetrischen Di-(arylamino)-oxybenzolen | |
| DE105736C (enrdf_load_stackoverflow) | ||
| DE664995C (de) | Verfahren zur Darstellung von Thiazthioniumchloriden | |
| DE2622838C2 (de) | Verfahren zur Herstellung von N-Alkylamino- und N,N-Dialkylamino- anthrachinonen | |
| DE205849C (enrdf_load_stackoverflow) | ||
| DE854802C (de) | Verfahren zur Herstellung von 4, 4'-Diaminodiphenylsulfoxyd | |
| DE749643C (de) | Verfahren zur Herstellung ungesaettigter Carbonsaeureamide | |
| DE954594C (de) | Verfahren zur Herstellung von Bisbiguaniden | |
| CH176360A (de) | Verfahren zur Darstellung von Kondensationsprodukten aus Phloroglucin und aromatischen Aminen. | |
| DE677897C (de) | Verfahren zur Herstellung von Salzen der Hexaacetatodioxycarbamidotriferribase | |
| DE38424C (de) | Verfahren zur Darstellung von substituirten Naphtylaminsulfosäuren und substituirten Naphtylaminen | |
| DE484664C (de) | Verfahren zur Darstellung von Sulfoderivaten der Oxyarylcarbonsaeurearylide | |
| DE319970C (de) | Verfahren zur Darstellung von p-Nitrophenylharnstoffderivaten | |
| DE128753C (enrdf_load_stackoverflow) | ||
| DE479227C (de) | Verfahren zur Herstellung der 2-Aminonaphthalin-3-carbonsaeure | |
| DE3115548A1 (de) | Verfahren zur herstellung von 1-alkylaminoanthrachinonen |