CH101089A - Process for the preparation of a vat dye of the indirubin series. - Google Patents
Process for the preparation of a vat dye of the indirubin series.Info
- Publication number
- CH101089A CH101089A CH101089DA CH101089A CH 101089 A CH101089 A CH 101089A CH 101089D A CH101089D A CH 101089DA CH 101089 A CH101089 A CH 101089A
- Authority
- CH
- Switzerland
- Prior art keywords
- indirubin
- series
- preparation
- vat dye
- brown
- Prior art date
Links
- CRDNMYFJWFXOCH-YPKPFQOOSA-N (3z)-3-(3-oxo-1h-indol-2-ylidene)-1h-indol-2-one Chemical class N/1C2=CC=CC=C2C(=O)C\1=C1/C2=CC=CC=C2NC1=O CRDNMYFJWFXOCH-YPKPFQOOSA-N 0.000 title claims description 3
- 239000000984 vat dye Substances 0.000 title description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 6
- 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 claims description 2
- 235000005811 Viola adunca Nutrition 0.000 claims description 2
- 240000009038 Viola odorata Species 0.000 claims description 2
- 235000013487 Viola odorata Nutrition 0.000 claims description 2
- 235000002254 Viola papilionacea Nutrition 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- 239000004753 textile Substances 0.000 claims description 2
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 claims 1
- 235000011121 sodium hydroxide Nutrition 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Nüpenfarbstoffes der Indirubinreihe. Es wurde gefunden, dass man zu einem neuen klaren, gelbstirIiigbraunenKüpenfarb- stoff dadurch gelangt, dass das in den Anna len der Chemie<B>388, 1919-,</B> Seite<B>10</B> beselirie- bene 2<B>-</B> 1-Naphtooxyihiophen mit<B>5 -</B> 7-Di- brornisatin kondensiert wird.
<I>Beispiel:</I> 200 Gewichtsteile 2<B>-</B> 1-Naplitooxythiophen und<B>305</B> Gewichtsteile<B>5 -</B> 7-Dibromisatin wer den in Eisessig gelöst, mit etwas konzen trierter Salzsiure zersetzt und eine Stunde lang im Wasserbad erhitzt; der Farbstoff bl wird abgesaugt und isoliert. Ausbeute<B>90</B> der Theorie.
Er bildet ein braunes, kristallinisches Pulver, das sieh in organischen Lösungsmit teln nur sehr schwer, in konzentrierter Schwe- felsätire wenig mit rotviole-Her, in Mono hydrat leicht mit blauvioleiter Farbe löst. Mit Ilydrosulfit und Natronlauge entsteht z# eine gelbe Küpe, aus welcher die Textilfaser in klaren, gelbstichig braunen Tönen -von ausgezeichneter Echtheit angefärbt wird.
Process for the preparation of a nub dye of the indirubin series. It has been found that a new, clear, yellowish-brown vat dye can be obtained by using the 2 described in Annals der Chemie <B> 388, 1919-, </B> page <B> 10 </B> <B> - </B> 1-naphtooxyihiophene is condensed with <B> 5 - </B> 7-dibrornisatin.
<I> Example: </I> 200 parts by weight of 2 <B> - </B> 1-naplitooxythiophene and <B> 305 </B> parts by weight of <B> 5 - </B> 7-dibromoisatin are dissolved in glacial acetic acid , decomposed with a little concentrated hydrochloric acid and heated in a water bath for one hour; the dye bl is filtered off and isolated. Yield <B> 90 </B> of theory.
It forms a brown, crystalline powder which, in organic solvents, dissolves only with great difficulty, in concentrated sulfuric acid it dissolves little with red violet, and in monohydrate easily with a blue-violet color. With Ilydrosulfite and sodium hydroxide solution, a yellow vat is created from which the textile fiber is dyed in clear, yellowish brown shades of excellent fastness.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE101089X | 1921-03-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH101089A true CH101089A (en) | 1923-09-01 |
Family
ID=5648765
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH101089D CH101089A (en) | 1921-03-26 | 1922-03-18 | Process for the preparation of a vat dye of the indirubin series. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH101089A (en) |
-
1922
- 1922-03-18 CH CH101089D patent/CH101089A/en unknown
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