CH210510A - Process for the preparation of a chromable dye of the triarylmethane series. - Google Patents
Process for the preparation of a chromable dye of the triarylmethane series.Info
- Publication number
- CH210510A CH210510A CH210510DA CH210510A CH 210510 A CH210510 A CH 210510A CH 210510D A CH210510D A CH 210510DA CH 210510 A CH210510 A CH 210510A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- chromable
- preparation
- triarylmethane series
- yellow
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title claims 2
- 239000000975 dye Substances 0.000 claims description 7
- 239000005711 Benzoic acid Substances 0.000 claims description 3
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 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
- C09B11/08—Phthaleins; Phenolphthaleins; Fluorescein
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 198713. Verfahren zur Herstellung eines ehromierbaren Farbstoffes der Triarylmethanreihe. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Herstellung eines chromier- baren Farbstoffes der Triarylmethanreihe, welches dadurch gekennzeichnet ist, dass man 2'.4'- Dioxy - 2 - benzoyl - (o - oxycarboxy)
-1- benzoesäure mit 1.3-Dioxynaphthalin kon densiert.
<I>Beispiel:</I> 40 Gewichtsteile 2'.4'-Dioxy-2-benzoyl- (o - oxycarboxy) -1- benzoesäure (erhältlich durch Kondensation von 1 Mol 5-Oxybenzol- 1.2.4-tricarbonsäure mit 1 Mol Resorcin, z. B.
durch Erhitzen dieser Stoffe bei etwa 100 bis 120 C in Gegenwart eines Lösungs- oder Verdünnungsmittels bis das Resorcin ver braucht ist) und 20 Gewichtsteile 1.3-Dioxy- naphthalin werden 4 Stunden auf 150 bis 160 C erhitzt. Die pulverisierte Schmelze wird in Bicarbonatlösung gelöst und die er haltene Lösung mit etwa 1 Gewichtsteil Tierkohle r/; Stunde gekocht. Aus der fil- trierten gelbroten Lösung wird der Farb stoff in der .Siedehitze mit verdünnter Salz säure ausgefällt.
Nach völligem Erkalten wird er wie üblich isoliert. Zur weiteren Reinigung kann er aus viel Eisessig oder Dioxan umkristallisiert werden. Der Farb stoff stellt ein gelbrotes, undeutlich kristalli nes Pulver dar. Er löst sich in Bicarbonat- lösung mit gelbroter Farbe und gelber Fluo reszenz. Wolle wird aus saurem Bade in klaren goldgelben Tönen gefärbt. Die chro- mierte Färbung ist braun und zeigt ver besserte Echtheitseigenschaften.
Additional patent to main patent No. 198713. Process for the production of an honorable dye of the triarylmethane series. The subject of this additional patent is a process for the production of a chromable dye of the triarylmethane series, which is characterized in that 2'.4'-dioxy - 2 - benzoyl - (o - oxycarboxy)
-1- benzoic acid condenses with 1,3-dioxynaphthalene.
<I> Example: </I> 40 parts by weight of 2'.4'-dioxy-2-benzoyl- (o - oxycarboxy) -1-benzoic acid (obtainable by condensation of 1 mole of 5-oxybenzene-1.2.4-tricarboxylic acid with 1 Moles of resorcinol, e.g.
by heating these substances at about 100 to 120 C in the presence of a solvent or diluent until the resorcinol is consumed) and 20 parts by weight of 1,3-dioxynaphthalene are heated to 150 to 160 C for 4 hours. The pulverized melt is dissolved in bicarbonate solution and the solution obtained with about 1 part by weight of animal charcoal r /; Cooked hour. The dye is precipitated from the filtered yellow-red solution at the boiling point with dilute hydrochloric acid.
After it has cooled completely, it is isolated as usual. For further purification it can be recrystallized from a lot of glacial acetic acid or dioxane. The color is a yellow-red, indistinct crystalline powder. It dissolves in bicarbonate solution with a yellow-red color and yellow fluorescence. Acid bath dyes wool in clear golden yellow tones. The chromed coloration is brown and shows improved fastness properties.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE210510X | 1936-03-27 | ||
| CH198713T | 1938-12-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH210510A true CH210510A (en) | 1940-07-15 |
Family
ID=25723151
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH210510D CH210510A (en) | 1936-03-27 | 1937-03-25 | Process for the preparation of a chromable dye of the triarylmethane series. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH210510A (en) |
-
1937
- 1937-03-25 CH CH210510D patent/CH210510A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH210509A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| DE483234C (en) | Process for the preparation of condensation products of the naphthostyril series | |
| DE631654C (en) | Process for the preparation of oxazine dyes | |
| DE610828C (en) | Process for the preparation of nitrogen-containing cyclic ketones | |
| DE522689C (en) | Process for the production of Kuepen dyes | |
| DE330550C (en) | Process for the preparation of methylene anthraquinone and its substitution products | |
| CH135478A (en) | Process for the preparation of a new dye. | |
| CH212579A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH212577A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH203054A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH144305A (en) | Process for the production of a vat dye of the pyrazole anthrone series. | |
| CH163280A (en) | Process for the production of a new vat dye. | |
| CH211033A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH210507A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH212576A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH191756A (en) | Process for the preparation of an acidic chromating dye of the anthraquinone series. | |
| CH187431A (en) | Process for the production of an acidic wool dye of the anthraquinone series. | |
| CH203047A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH109641A (en) | Process for the production of a new vat dye. | |
| CH191748A (en) | Process for the preparation of an acidic chromating dye of the anthraquinone series. | |
| CH106133A (en) | Process for the preparation of 2,3-thionaphthisatin. | |
| CH203053A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH210506A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
| CH192851A (en) | Process for the preparation of a chromable monoazo dye. | |
| CH109648A (en) | Process for the production of a new vat dye. |