AT50291B - Process for the preparation of nitrogen-containing anthraquinone derivatives. - Google Patents
Process for the preparation of nitrogen-containing anthraquinone derivatives.Info
- Publication number
- AT50291B AT50291B AT50291DA AT50291B AT 50291 B AT50291 B AT 50291B AT 50291D A AT50291D A AT 50291DA AT 50291 B AT50291 B AT 50291B
- Authority
- AT
- Austria
- Prior art keywords
- sep
- nitrogen
- preparation
- anthraquinone derivatives
- containing anthraquinone
- Prior art date
Links
- -1 nitrogen-containing anthraquinone Chemical class 0.000 title description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 title 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 2
- KXOGXZAXERYOTC-UHFFFAOYSA-N 1-amino-4-methoxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2OC KXOGXZAXERYOTC-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 description 1
- ZLCUIOWQYBYEBG-UHFFFAOYSA-N 1-Amino-2-methylanthraquinone Chemical compound C1=CC=C2C(=O)C3=C(N)C(C)=CC=C3C(=O)C2=C1 ZLCUIOWQYBYEBG-UHFFFAOYSA-N 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 235000005811 Viola adunca Nutrition 0.000 description 1
- 240000009038 Viola odorata Species 0.000 description 1
- 235000013487 Viola odorata Nutrition 0.000 description 1
- 235000002254 Viola papilionacea Nutrition 0.000 description 1
- 244000172533 Viola sororia Species 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
Landscapes
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Description
<Desc/Clms Page number 1>
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<tb>
<tb> Produkt <SEP> aus: <SEP> Aussehen: <SEP> Farbe <SEP> der <SEP> Lösung <SEP> Farbe <SEP> der <SEP> Lösung <SEP> Farbe <SEP> der <SEP> Lösung
<tb> in <SEP> Pyridin: <SEP> in <SEP> konzentrierter <SEP> in <SEP> 65prozentigem
<tb> H2SO4 <SEP> von <SEP> 90 C <SEP> Oleum
<tb> 1,4-Diaminoanthrachinon+ <SEP> dunkelblaue <SEP> blau <SEP> rotviolett <SEP> blau
<tb> +Äthylenoxyd. <SEP> ... <SEP> .. <SEP> ..... <SEP> Prismen
<tb> 1-Amino-4-methoxyanthrachinon+ <SEP> bronzeglänzende <SEP> rotviolett <SEP> gelbbraun <SEP> blauviolett
<tb> +Äthylenoxyd.............. <SEP> Kristalle
<tb> Kristalleiseasig
<tb> enthaltende
<tb> 1-Amino-2-methylanthrachinon <SEP> + <SEP> Prismen, <SEP> die <SEP> beim <SEP> blaustichig <SEP> gelb <SEP> gelb
<tb> + <SEP> Äthylenoxyd..... <SEP> .......
<SEP> Trocknen <SEP> ver- <SEP> rot
<tb> wittern
<tb> 1.5-Diaminoanthrachinon <SEP> + <SEP> Glyzid <SEP> branne <SEP> Kristalle <SEP> rot <SEP> blanviolett <SEP> grünstichig
<tb> 1-Am <SEP> noanthrachinon <SEP> + <SEP> Äthylen- <SEP> rote <SEP> Kristalle <SEP> rot <SEP> violettrot <SEP> violett
<tb> oxyd. <SEP> .....................
<tb>
1-Amino-4-methoxyanthrachinon+
<tb> + <SEP> Propylenoxyd <SEP> .. <SEP> .. <SEP> .... <SEP> .
<tb>
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<tb>
<tb> Product <SEP> from: <SEP> Appearance: <SEP> Color <SEP> of the <SEP> solution <SEP> Color <SEP> of the <SEP> solution <SEP> Color <SEP> of the <SEP> solution
<tb> in <SEP> pyridine: <SEP> in <SEP> concentrated <SEP> in <SEP> 65 percent
<tb> H2SO4 <SEP> from <SEP> 90 C <SEP> oleum
<tb> 1,4-diaminoanthraquinone + <SEP> dark blue <SEP> blue <SEP> red-violet <SEP> blue
<tb> + ethylene oxide. <SEP> ... <SEP> .. <SEP> ..... <SEP> prisms
<tb> 1-Amino-4-methoxyanthraquinone + <SEP> shiny bronze <SEP> red-violet <SEP> yellow-brown <SEP> blue-violet
<tb> + ethylene oxide .............. <SEP> crystals
<tb> Kristalliseasig
<tb> containing
<tb> 1-Amino-2-methylanthraquinone <SEP> + <SEP> prisms, <SEP> the <SEP> with <SEP> has a blue cast <SEP> yellow <SEP> yellow
<tb> + <SEP> ethylene oxide ..... <SEP> .......
<SEP> drying <SEP> turns <SEP> red
<tb> smell
<tb> 1.5-diaminoanthraquinone <SEP> + <SEP> glycid <SEP> burn <SEP> crystals <SEP> red <SEP> blanviolet <SEP> greenish tint
<tb> 1-Am <SEP> noanthraquinone <SEP> + <SEP> ethylene- <SEP> red <SEP> crystals <SEP> red <SEP> violet-red <SEP> violet
<tb> oxide. <SEP> .....................
<tb>
1-amino-4-methoxyanthraquinone +
<tb> + <SEP> propylene oxide <SEP> .. <SEP> .. <SEP> .... <SEP>.
<tb>
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Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE50291X | 1910-01-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT50291B true AT50291B (en) | 1911-10-25 |
Family
ID=5626598
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT50291D AT50291B (en) | 1910-01-10 | 1910-12-01 | Process for the preparation of nitrogen-containing anthraquinone derivatives. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT50291B (en) |
-
1910
- 1910-12-01 AT AT50291D patent/AT50291B/en active
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