DE88085C - - Google Patents
Info
- Publication number
- DE88085C DE88085C DENDAT88085D DE88085DA DE88085C DE 88085 C DE88085 C DE 88085C DE NDAT88085 D DENDAT88085 D DE NDAT88085D DE 88085D A DE88085D A DE 88085DA DE 88085 C DE88085 C DE 88085C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- dibenzylaniline
- dyes
- tetramethyldiamidodiphenylmethane
- oxidation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000002253 acid Substances 0.000 claims description 10
- 239000000975 dye Substances 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 2
- BRCZRSQATONSIY-UHFFFAOYSA-N (2,3-dibenzylphenyl)-sulfosulfamic acid Chemical compound C(C1=CC=CC=C1)C=1C(=C(N(S(=O)(=O)O)S(=O)(=O)O)C=CC1)CC1=CC=CC=C1 BRCZRSQATONSIY-UHFFFAOYSA-N 0.000 claims 1
- 235000005811 Viola adunca Nutrition 0.000 claims 1
- 240000009038 Viola odorata Species 0.000 claims 1
- 235000013487 Viola odorata Nutrition 0.000 claims 1
- 235000002254 Viola papilionacea Nutrition 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 238000005987 sulfurization reaction Methods 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- SLXZZXJPFRYIKN-UHFFFAOYSA-N benzyl-(2-ethylphenyl)sulfamic acid Chemical compound CCC1=CC=CC=C1N(S(O)(=O)=O)CC1=CC=CC=C1 SLXZZXJPFRYIKN-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 2
- -1 sodium dibenzylaniline monosulfonic acid Chemical compound 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FBEHFRAORPEGFH-UHFFFAOYSA-N Allyxycarb Chemical compound CNC(=O)OC1=CC(C)=C(N(CC=C)CC=C)C(C)=C1 FBEHFRAORPEGFH-UHFFFAOYSA-N 0.000 description 1
- FRHAXDBAIRLBBC-UHFFFAOYSA-M C(C1=CC=CC=C1)C1=C(N(S(=O)(=O)[O-])CC2=CC=CC=C2)C=CC=C1.[Na+] Chemical compound C(C1=CC=CC=C1)C1=C(N(S(=O)(=O)[O-])CC2=CC=CC=C2)C=CC=C1.[Na+] FRHAXDBAIRLBBC-UHFFFAOYSA-M 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- ISGXOWLMGOPVPB-UHFFFAOYSA-N n,n-dibenzylaniline Chemical compound C=1C=CC=CC=1CN(C=1C=CC=CC=1)CC1=CC=CC=C1 ISGXOWLMGOPVPB-UHFFFAOYSA-N 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 210000002268 wool Anatomy 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
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/12—Amino derivatives of triarylmethanes without any OH group bound to an aryl nucleus
- C09B11/16—Preparation from diarylketones or diarylcarbinols, e.g. benzhydrol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE88085C true DE88085C (en:Method) |
Family
ID=360002
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT88085D Active DE88085C (en:Method) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE88085C (en:Method) |
-
0
- DE DENDAT88085D patent/DE88085C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE620462C (de) | Verfahren zur Herstellung von Farbstoffen der Triarylmethanreihe | |
| DE88085C (en:Method) | ||
| DE98012C (en:Method) | ||
| DE98321C (en:Method) | ||
| DE65017C (de) | Verfahren zur Darstellung blauer Triphenylmethanfarbstoffe aus der Disulfosäure des Tetramethyldiamidodiphenylmethans | |
| DE97638C (en:Method) | ||
| DE574021C (de) | Verfahren zur Herstellung von Triarylmethanfarbstoffen | |
| DE121836C (en:Method) | ||
| DE402640C (de) | Verfahren zur Herstellung von Chlorderivaten der Dibenzanthrone | |
| DE254743C (en:Method) | ||
| DE63026C (de) | Verfahren zur Darstellung grüner basischer Farbstoffe der Triphenylmethanreihe | |
| DE583936C (de) | Verfahren zur Herstellung von 1íñ4-Diamino-2-aryloxyanthrachinon-3-sulfonsaeuren | |
| DE289112C (en:Method) | ||
| DE98072C (en:Method) | ||
| DE128086C (en:Method) | ||
| DE146655C (en:Method) | ||
| DE171684C (en:Method) | ||
| DE62574C (de) | Verfahren zur Darstellung neuer rother basischer Farbstoffe der Triphenylmethan-] reihe | |
| DE91315C (en:Method) | ||
| DE186989C (en:Method) | ||
| DE96230C (en:Method) | ||
| DE175826C (en:Method) | ||
| DE117587C (en:Method) | ||
| DE602095C (de) | Verfahren zur Darstellung von indigoiden Farbstoffen | |
| DE73717C (de) | Verfahren zur Darstellung von • blauen Farbstoffen, den Sulfosäuren der secundäre.n Diamidoditolyloxyphenylcarbinole |