CH190338A - Process for the preparation of a quinophthalone sulfonic acid. - Google Patents
Process for the preparation of a quinophthalone sulfonic acid.Info
- Publication number
- CH190338A CH190338A CH190338DA CH190338A CH 190338 A CH190338 A CH 190338A CH 190338D A CH190338D A CH 190338DA CH 190338 A CH190338 A CH 190338A
- Authority
- CH
- Switzerland
- Prior art keywords
- quinophthalone
- sulfonic acid
- preparation
- heated
- equivalent amount
- Prior art date
Links
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 title claims description 12
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims 1
- 229910052753 mercury Inorganic materials 0.000 claims 1
- FWFGVMYFCODZRD-UHFFFAOYSA-N oxidanium;hydrogen sulfate Chemical compound O.OS(O)(=O)=O FWFGVMYFCODZRD-UHFFFAOYSA-N 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
Landscapes
- Quinoline Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung einer Chinophthalonsulfosäure. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung einer Chinophtha- lonsulfosäure, welches dadurch gekennzeich net ist, dass man Chinophthalon mit der äqui-. valenten Menge eines Sulfierungsmittels er hitzt.
<I>Beispiel:</I> 27,2 Gewichtsteile Chinophthalon werden mit 15 Gewichtsteilen ll,lonohydrat zusammen verrieben. Dabei bildet sich unter schwacher spontaner Erwärmung ,das Sulfat des Chino- phthalons, welches schnell zu einer festen, roten, kristallinen Masse erstarrt. Diese wird bei einem Druck von 2 bis 3 mm Hg 4 Stun den lang auf<B>190'</B> C erwärmt. Dabei wird die anfangs ziemlich diinnflüssige und bla sige Schmelze immer zäher. Nach dem Er kalten wird die erstarrte Masse gepulvert und mit heissem )Vasser aufgekocht und so in Lösung gebracht.
Die heisse Flüssigkeit wird durch Filtration geklärt. Durch Aus sahen mit Kochsalz erhält man aus dem Fil trat die Chinophthalonsulfosäure in guter Ausbeute. Sie bildet ein hellgelbes, in Was- ser lösliches Pulver, das Wolle gut egalisie rend in gelben Tönen aus saurem Bade färbt.
Process for the preparation of a quinophthalone sulfonic acid. The subject of this additional patent is a process for the preparation of a quinophthalone sulfonic acid, which is characterized in that one quinophthalone with the equi-. equivalent amount of a sulfonating agent he heats.
<I> Example: </I> 27.2 parts by weight of quinophthalone are triturated together with 15 parts by weight of II ionohydrate. The sulfate of quinophthalone is formed with weak spontaneous heating, which quickly solidifies to a solid, red, crystalline mass. This is heated to <B> 190 '</B> C for 4 hours at a pressure of 2 to 3 mm Hg. The initially rather thin and pale melt becomes increasingly viscous. After it has cooled down, the solidified mass is powdered and boiled with hot water to dissolve it.
The hot liquid is clarified by filtration. By looking with common salt, the quinophthalone sulfonic acid is obtained from the fil in good yield. It forms a light yellow, water-soluble powder that dyes wool in yellow shades from acidic baths, smoothly and evenly.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE185959X | 1934-08-09 | ||
| CH185959T | 1935-08-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH190338A true CH190338A (en) | 1937-04-15 |
Family
ID=25721327
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH190338D CH190338A (en) | 1934-08-09 | 1935-08-08 | Process for the preparation of a quinophthalone sulfonic acid. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH190338A (en) |
-
1935
- 1935-08-08 CH CH190338D patent/CH190338A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE665599C (en) | Process for the preparation of quinophthalone monosulfonic acids | |
| CH312530A (en) | Process for making a pyridazone. | |
| AT99014B (en) | Process for the preparation of compounds of 4-dimethylamino-2,3-dimethyl-1-phenil-5-pyrazolone. | |
| DE665774C (en) | Process for the production of phenols | |
| DE589638C (en) | Process for the preparation of 1íñ4-diaminoanthraquinone-2íñ3íñ? -Trisulfonic acids | |
| CH185959A (en) | Process for the preparation of a quinophthalone sulfonic acid. | |
| AT111847B (en) | Process for the preparation of compounds from C, C-disubstituted barbituric acids with 1-phenyl-2,3-dimethyl-4-dimethylamino-5-pyrazolone. | |
| DE318898C (en) | Process for the preparation of ethyl acetate from acetaldehyde | |
| DE547984C (en) | Process for the preparation of compounds of the alkali salts C, C-disubstituted barbituric acids with pyrazolones | |
| CH142341A (en) | Process for the preparation of 2-chloro-4- (di- (oxyethyl)) -amino-1-oxybenzene. | |
| CH261821A (en) | Process for the preparation of a substituted 2,4-diamino-1,3,5-triazine. | |
| CH230438A (en) | Process for producing a benzenesulfonic acid amide compound. | |
| CH199044A (en) | Process for the preparation of a p-phenanthroline derivative. | |
| CH154173A (en) | Process for the preparation of 5,6-dimethoxy-8-aminoquinoline. | |
| DE1167333B (en) | Process for the production of naphthalene-2-sulfonic acid | |
| CH202158A (en) | Process for the preparation of a diphenyl series hydrazine. | |
| CH105411A (en) | Process for preparing a barbituric acid compound. | |
| CH191165A (en) | Process for the preparation of a new monoazo dye. | |
| CH105867A (en) | Process for preparing a barbituric acid compound. | |
| CH206628A (en) | Process for the preparation of a thiazolium compound. | |
| CH234253A (en) | Process for the preparation of a sulfonamide compound. | |
| CH147685A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
| CH202162A (en) | Process for the preparation of a new aminoketone. | |
| CH105868A (en) | Process for preparing a barbituric acid compound. | |
| CH147692A (en) | Process for the preparation of a product which can be used as an azo dye component. |