CH148689A - Process for the preparation of a vat dye. - Google Patents
Process for the preparation of a vat dye.Info
- Publication number
- CH148689A CH148689A CH148689DA CH148689A CH 148689 A CH148689 A CH 148689A CH 148689D A CH148689D A CH 148689DA CH 148689 A CH148689 A CH 148689A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- condensation
- preparation
- diaminobenzene
- methyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title claims description 4
- 239000000984 vat dye Substances 0.000 title claims description 4
- 238000009833 condensation Methods 0.000 claims description 7
- 230000005494 condensation Effects 0.000 claims description 7
- 239000000975 dye Substances 0.000 claims description 6
- ZZLCFHIKESPLTH-UHFFFAOYSA-N 4-Methylbiphenyl Chemical compound C1=CC(C)=CC=C1C1=CC=CC=C1 ZZLCFHIKESPLTH-UHFFFAOYSA-N 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 229920000742 Cotton Polymers 0.000 claims description 2
- 150000008064 anhydrides Chemical class 0.000 claims description 2
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 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 Küpenfarbstoffes. Gegenstand dieses Patentes ist ein Ver fahren zur Darstellung eines Küpenfarb- stoffes, -welches dadurch gekennzeichnet ist, dass man Naphtoylen-methyl-benzimidazol- peri-dicarbonsäureanhydrid, das durch Kon densation von Naphtoylen-4. 5-diäthylindan- dion-1.8-dicarbonsäureanhydrid mit 4-Me- thyl-1 .
2-diaminobenzol, darauffolgende Auf- spaltung mit Alkali und Oxydation erhält lich ist, mit 1. 2-Diaminobenzol kondensiert. <I>Beispiel</I> Kondensiert man Naphtoylen-methyl-benz- imidazol-peri-dicarbonsäureanhydrid folgen der Formel:
EMI0001.0018
das durch Kondensation von Naphtoylen-4.5- diäthylindandion-1. 8-dicarbonsäureanhydrid mit 4-Methyl-1. 2-diaminobenzol, darauffol gende Aufspaltung mit Alkali und Oxydation erhältlich ist, mit 1. 2-Diaminobenzol, so er hält man einen Farbstoff, der aus olivgrüner Hydrosulfitküpe Baumwolle in roten Tönen anfärbt. Die Echtheitseigenschaften des Farbstoffes sind gut.
Die Kondensation zu dem entsprechenden Farbstoff wird zweckmässig in Lösungsmit teln bezw. Verdünnungsmitteln, wie Eisessig, Nitrobenzol, einem Gemisch von beiden, fer ner zum Beispiel Py ridin, eventuell auch Wasser (im Autoklaven) durchgeführt.
Die Kondensation erfolgt zweckmässig durch Erwärmen auf Temperaturen zwischen 100 C und zirka 130 C.
Process for the preparation of a vat dye. The subject of this patent is a process for the preparation of a vat dye, which is characterized in that naphthoylene-methyl-benzimidazole peri-dicarboxylic acid anhydride, which is produced by condensation of naphthoylene-4. 5-diethylindandione-1,8-dicarboxylic acid anhydride with 4-methyl-1.
2-diaminobenzene, subsequent splitting with alkali and oxidation is obtainable, condensed with 1. 2-diaminobenzene. <I> Example </I> If naphthoylene-methyl-benz-imidazole-peri-dicarboxylic acid anhydride is condensed, follow the formula:
EMI0001.0018
that by condensation of naphthylene-4,5-diethylindandione-1. 8-dicarboxylic anhydride with 4-methyl-1. 2-diaminobenzene, subsequent splitting with alkali and oxidation is available, with 1. 2-diaminobenzene, so he holds a dye that dyes cotton from olive-green hydrosulfite vat in red shades. The fastness properties of the dye are good.
The condensation to the corresponding dye is expediently BEZW in solvents. Diluents, such as glacial acetic acid, nitrobenzene, a mixture of both, also for example pyridine, possibly also water (in an autoclave).
The condensation is expediently carried out by heating to temperatures between 100 C and about 130 C.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE148689X | 1928-06-18 | ||
| CH143998T | 1929-06-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH148689A true CH148689A (en) | 1931-07-31 |
Family
ID=25714398
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH148689D CH148689A (en) | 1928-06-18 | 1929-06-05 | Process for the preparation of a vat dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH148689A (en) |
-
1929
- 1929-06-05 CH CH148689D patent/CH148689A/en unknown
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