DE241822C - - Google Patents
Info
- Publication number
- DE241822C DE241822C DENDAT241822D DE241822DA DE241822C DE 241822 C DE241822 C DE 241822C DE NDAT241822 D DENDAT241822 D DE NDAT241822D DE 241822D A DE241822D A DE 241822DA DE 241822 C DE241822 C DE 241822C
- Authority
- DE
- Germany
- Prior art keywords
- aminoanthraquinone
- phosgene
- hydrochloric acid
- chloride
- anthraquinonylurea
- 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
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 23
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 23
- XOGPDSATLSAZEK-UHFFFAOYSA-N 2-Aminoanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(N)=CC=C3C(=O)C2=C1 XOGPDSATLSAZEK-UHFFFAOYSA-N 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 18
- 239000000203 mixture Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000000725 suspension Substances 0.000 description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 5
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 5
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- 238000003756 stirring Methods 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- JZLDXVVDXPWOBH-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione hydrochloride Chemical compound Cl.O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N JZLDXVVDXPWOBH-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- HFWAYUQPWDTNGS-UHFFFAOYSA-N NC(NC(C=C1)=CC(C(C2=CC=CC=C22)=O)=C1C2=O)=O.Cl Chemical compound NC(NC(C=C1)=CC(C(C2=CC=CC=C22)=O)=C1C2=O)=O.Cl HFWAYUQPWDTNGS-UHFFFAOYSA-N 0.000 description 1
- QONRLFCAYFCGBW-UHFFFAOYSA-N NC(NC1=CC=CC(C(C2=CC=CC=C22)=O)=C1C2=O)=O.Cl Chemical class NC(NC1=CC=CC(C(C2=CC=CC=C22)=O)=C1C2=O)=O.Cl QONRLFCAYFCGBW-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- WOKZFJICKMOZLE-UHFFFAOYSA-N ethyl n-(9,10-dioxoanthracen-1-yl)carbamate Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)OCC WOKZFJICKMOZLE-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003673 urethanes Chemical class 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/36—Dyes with acylated amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE241822T | 1909-05-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE241822C true DE241822C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Family
ID=8898062
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT241822D Active DE241822C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1909-05-12 |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE241822C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
| FR (1) | FR415789A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
-
0
- DE DENDAT241822D patent/DE241822C/de active Active
-
1910
- 1910-05-10 FR FR415789D patent/FR415789A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR415789A (fr) | 1910-10-04 |
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