CH93492A - Process for the preparation of a dye of the phenyldinaphtylmethane series. - Google Patents
Process for the preparation of a dye of the phenyldinaphtylmethane series.Info
- Publication number
- CH93492A CH93492A CH93492DA CH93492A CH 93492 A CH93492 A CH 93492A CH 93492D A CH93492D A CH 93492DA CH 93492 A CH93492 A CH 93492A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- acid
- preparation
- phenyldinaphtylmethane
- series
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 238000010367 cloning Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 235000011121 sodium hydroxide Nutrition 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LVZPKYYPPLUECL-UHFFFAOYSA-N 1-chloro-4-(trichloromethyl)benzene Chemical compound ClC1=CC=C(C(Cl)(Cl)Cl)C=C1 LVZPKYYPPLUECL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- -1 carbonic acid 4-chlorobenzene trichloride Chemical compound 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000003756 stirring 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
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/06—Hydroxy derivatives of triarylmethanes in which at least one OH group is bound to an aryl nucleus and their ethers or esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Description
Verfahren zur Herstellung eines Farbstoffe-s der Plienyldinahhtylnietlianreihe. Es wurde- gefunden, dass, wenn man a12' 1-Naphtol-2-e,rbonsäiire 4-Clilorbenzoltri- chlorid in (-T'e"enwart eines säurebindenden Mittels.
vorzugsweise unter Zugabe eines Katalysators, einwirken lässt, ein neuer Farb- toff erhalten wird. Dieser Farbstoff gibt s<B>s</B> auf Wolle, aus saurein Bade gefärbt eine graue Färbung, welche beine Nachchroniieren in ein reines. N- orzüglicli echtes Grün über geht.
Beispiel: 752 Teile 1-Naphtol-2-carlionsäure -,ver- den - in 1900 Teilen Natronlauge von 30 Gew. und 500 Teilen -\Vasser gelöst. Hier auf gibt inan ! 34 Teile 4-Clilorbenzotrichlorid und 0,5 Teile Kupfer hinzu und rührt so lange, bis alles Benzotriclilorid verschwunden ist.
Das Natriumsalz des gebildeten Farb stoffes wird durch Aussalzen aus dein mit Wasser verdünnten Reaktionsgemisch abge schieden.
Process for the preparation of a dye of the Plienyldinahhtylnietlian reason. It has been found that if one converts a12 '1-naphthol-2-e, carbonic acid 4-chlorobenzene trichloride into (-T'e "in the presence of an acid-binding agent.
preferably with the addition of a catalyst, a new dye is obtained. This dye gives s <B> s </B> on wool, dyed from acidic bath a gray color, which is followed by post-chronizing into a pure. N- orzüglicli real green goes over.
Example: 752 parts of 1-naphthol-2-carlionic acid - dissolved in 1900 parts of 30% by weight sodium hydroxide solution and 500 parts of water. Give up here! Add 34 parts of 4-chlorobenzotrichloride and 0.5 part of copper and stir until all the benzotricliloride has disappeared.
The sodium salt of the dye formed is separated out by salting out the reaction mixture diluted with water.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH93492T | 1921-01-18 | ||
| CH92406T | 1921-01-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH93492A true CH93492A (en) | 1922-03-01 |
Family
ID=25704488
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH93492D CH93492A (en) | 1921-01-18 | 1921-01-18 | Process for the preparation of a dye of the phenyldinaphtylmethane series. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH93492A (en) |
-
1921
- 1921-01-18 CH CH93492D patent/CH93492A/en unknown
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