AT24655B - Process for the preparation of 1,5- and 1,8-nitroanthraquinone sulfonic acid. - Google Patents
Process for the preparation of 1,5- and 1,8-nitroanthraquinone sulfonic acid.Info
- Publication number
- AT24655B AT24655B AT24655DA AT24655B AT 24655 B AT24655 B AT 24655B AT 24655D A AT24655D A AT 24655DA AT 24655 B AT24655 B AT 24655B
- Authority
- AT
- Austria
- Prior art keywords
- sep
- sulfonic acid
- nitroanthraquinone
- preparation
- red
- Prior art date
Links
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 title claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 230000000802 nitrating effect Effects 0.000 claims 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- FGHSTPNOXKDLKU-UHFFFAOYSA-N nitric acid;hydrate Chemical compound O.O[N+]([O-])=O FGHSTPNOXKDLKU-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
EMI1.1
EMI1.2
EMI1.3
<tb>
<tb> Methylamidoanthrachinonsulfosäure <SEP> 1.5 <SEP> 1.8
<tb> Lösung <SEP> in <SEP> H2 <SEP> O <SEP> blaustichig <SEP> rot <SEP> blaustichig <SEP> rot
<tb> kenz. <SEP> H2 <SEP> SO4 <SEP> schwach <SEP> gelblich <SEP> schwach <SEP> gelblich
<tb> 45% <SEP> Gleum <SEP> rot <SEP> violettrot
<tb> ! <SEP> Eiseas <SEP> : <SEP> g <SEP> rot <SEP> rot
<tb>
<Desc/Clms Page number 2>
Statt in Schwefelsäure kann man beispielsweise auch in hochprozentiger Salpeter- säure allein oder in Salpetersituremonohydrat nitrieren, wie im folgenden Beispiel erläutert wird.
Beispiel 2. 40 kg Anthrachinon-α-monosulfosaures Kalium werden in 100 kg Salpetersäure von 480 usé. eingetragen und das Ganze unter Rühren zehn Stunden lang auf 80-900 erwärmt. Man versetzt bierauf mit 5-10 kg Wasser und lässt erkalten, wobei sich die 1.5-Nitroanthrachinonsulfosäure abscheidet. Dieselbe wird abfiltriert und aus dem Filtrat durch weiteren Wasserzusatz die 1. 8-NitroBulfosäure abgeschieden.
<Desc / Clms Page number 1>
EMI1.1
EMI1.2
EMI1.3
<tb>
<tb> Methylamidoanthraquinone sulfonic acid <SEP> 1.5 <SEP> 1.8
<tb> Solution <SEP> in <SEP> H2 <SEP> O <SEP> bluish tint <SEP> red <SEP> bluish tint <SEP> red
<tb> kenz. <SEP> H2 <SEP> SO4 <SEP> weakly <SEP> yellowish <SEP> weakly <SEP> yellowish
<tb> 45% <SEP> Gleum <SEP> red <SEP> violet red
<tb>! <SEP> Eiseas <SEP>: <SEP> g <SEP> red <SEP> red
<tb>
<Desc / Clms Page number 2>
Instead of in sulfuric acid, for example, nitration can also be carried out in high-percentage nitric acid alone or in nitric acid monohydrate, as is explained in the following example.
Example 2. 40 kg of anthraquinone-α-monosulfonate of potassium are dissolved in 100 kg of nitric acid of 480 usé. entered and the whole thing heated to 80-900 for ten hours while stirring. 5-10 kg of water are added to the beer and the mixture is allowed to cool, the 1,5-nitroanthraquinone sulfonic acid separating out. The same is filtered off and the 1,8-nitro-sulfonic acid is separated off from the filtrate by adding more water.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1903164293D DE164293C (en) | 1903-01-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT24655B true AT24655B (en) | 1906-06-25 |
Family
ID=5684222
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT24655D AT24655B (en) | 1903-01-17 | 1905-09-25 | Process for the preparation of 1,5- and 1,8-nitroanthraquinone sulfonic acid. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT24655B (en) |
-
1905
- 1905-09-25 AT AT24655D patent/AT24655B/en active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AT24655B (en) | Process for the preparation of 1,5- and 1,8-nitroanthraquinone sulfonic acid. | |
| DE478844C (en) | Process for the production of 6-nitrosafrol | |
| AT96799B (en) | Process for the preparation of 3-10 perylene quinone. | |
| AT21606B (en) | Process for the preparation of m-Tolylsemicarbazide. | |
| AT29054B (en) | Process for the preparation of a green vat dye. | |
| AT64815B (en) | Process for the preparation of quinizarin. | |
| AT119495B (en) | Process for the preparation of perylenetetracarboxylic anhydride. | |
| AT24753B (en) | Process for the introduction of hydroxyl groups in anthraquinone and its derivatives. | |
| DE647406C (en) | Process for the preparation of aminoacylaminoanthraquinones | |
| DE632130C (en) | Process for the preparation of diarylguanidines | |
| AT22658B (en) | ) Process for the preparation of a blue dye of the anthracene series. | |
| DE611112C (en) | Process for the preparation of 1íñ4-dihaloanthraquinone-2-carboxylic acids | |
| DE899200C (en) | Process for the preparation of 2, 7-diaminodibenzothiophendioxyd-3, 6-disulfonic acid | |
| US1314920A (en) | Chester e | |
| DE578503C (en) | Process for the reduction of connectable, water-insoluble nitro compounds | |
| AT21546B (en) | Process for the preparation of 1.5- and 1.8-anthraquinone disulfonic acid. | |
| AT53786B (en) | Process for the representation of tri- and tetrahalogenindigo. | |
| AT102533B (en) | Process for the production of vat dyes. | |
| AT79023B (en) | Process for the preparation of pure, high-grade nitric acid from gases containing nitrogen oxides. | |
| AT93323B (en) | Process for the production of trinitroresorzin. | |
| AT26616B (en) | Process for the preparation of a yellow anthracene dye. | |
| AT69808B (en) | Process for the preparation of carbazole monosulfonic acids. | |
| CH176028A (en) | Process for the preparation of 2-amino-3-chloroanthraquinone. | |
| AT87643B (en) | Process for the production of benzoic acid by the oxidation of toluene with chromosulfuric acid. | |
| DE101220C (en) |