CH230636A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH230636A CH230636A CH230636DA CH230636A CH 230636 A CH230636 A CH 230636A CH 230636D A CH230636D A CH 230636DA CH 230636 A CH230636 A CH 230636A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- condensed
- preparation
- azo dye
- azo
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- 239000000987 azo dye Substances 0.000 title description 2
- 239000000975 dye Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229920000742 Cotton Polymers 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims 1
- 239000003575 carbonaceous material Substances 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- IPOFQEDKXYAPBX-UHFFFAOYSA-N 1,4-diaminocyclohexa-2,4-diene-1-sulfonic acid Chemical compound NC1=CCC(N)(S(O)(=O)=O)C=C1 IPOFQEDKXYAPBX-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B56/00—Azo dyes containing other chromophoric systems
- C09B56/04—Stilbene-azo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 225559. Verfahren zur Herstellung eines Azofarbstoffes. Gegenstand vorliegender Erfindung ist ein Verfahren zur HeTstallung eines Azo@farb- stoffes. Das Varfahren ist dadurch gekenn- zeichnet, dass mann 4,4'-Ilinibro3tilben-2,
2'- disulfonsäure in natronalkalis.cher Lösung zunächst mit 1 Mal 1,4-Diamino-benzol- eu,fons!äure bei einer Temperatur unter 50 kondensiert und dann mit einem weiteren Mod 1,4 - D,i@a:minobenzolsulfonsäure bei höherer Temperatur zum zweiten Mal kondensiert.
Der neue Farbstoff stellt ein dunkles Pulver dar, das sich in Wassier mit gelber Farbe löst und Baumwolle in ,gelben Tönen färbt. Er soll vor allem als Zwischenprodukt zum Aufbau anderer Farbstoffe verwendet werden.
<I>Beispiel:</I> 43 Gewichtsteile 4,4'-Dinitriostilben-2,2'- d;iisulfons,äure werden in ungefähr 700 Ge- wichts@teilen 5 %iger Natronlauige gelöst, mit 19 Gewichtsteilen 1,4-Diaminobenz.olsulfon- eäure vews,etzt und ungefähr 12 Stunden bei ,einer Temperatur von 45 gehalten.
Dias aus- gefallene und isolierte Monokondensations- produkt wird mit weiteren 19 Gewichtsteilen 1,4-D,iamimob,enzolsudf on.säure in 750 Ge- wichtsteiIen 5 % iger Natronlauge etwa 10 Stunden auf 80-85 erhitzt.
Nach diesem Zeit ist in guter Ausbeute der Farbstoff fol gender Konstitution ausgefallen:
EMI0001.0080
Additional patent to main patent no. 225559. Process for the production of an azo dye. The present invention relates to a process for the production of an Azo® dye. The method is characterized by the fact that 4,4'-ilinibro3tilbene-2,
2'-disulfonic acid in natronalkalis.cher solution first condensed with 1,4-diamino-benzenesulfonic acid at a temperature below 50 and then with a further mod 1,4-D, i @ a: minobenzenesulfonic acid condensed for the second time at a higher temperature.
The new dye is a dark powder that dissolves in water with a yellow color and dyes cotton in yellow tones. It is primarily intended to be used as an intermediate in the synthesis of other dyes.
<I> Example: </I> 43 parts by weight of 4,4'-dinitriostilbene-2,2'- d; iisulfonic acid are dissolved in about 700 parts by weight of 5% sodium hydroxide, with 19 parts by weight of 1,4- Diaminobenzenesulfonic acid vews, etched, and kept at a temperature of 45 for about 12 hours.
The precipitated and isolated monocondensation product is heated to 80-85 for about 10 hours with a further 19 parts by weight of 1,4-D, iamimob, enzolsudfon.äure in 750 parts by weight of 5% sodium hydroxide solution.
After this time, the dye has precipitated in good yield with the following constitution:
EMI0001.0080
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE230636X | 1940-04-29 | ||
| CH225559T | 1941-08-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH230636A true CH230636A (en) | 1944-01-15 |
Family
ID=25726913
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH230636D CH230636A (en) | 1940-04-29 | 1941-08-15 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH230636A (en) |
-
1941
- 1941-08-15 CH CH230636D patent/CH230636A/en unknown
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