GB748715A - Manufacture of arylamino-aminoalkyl-compounds - Google Patents
Manufacture of arylamino-aminoalkyl-compoundsInfo
- Publication number
- GB748715A GB748715A GB23333/53A GB2333353A GB748715A GB 748715 A GB748715 A GB 748715A GB 23333/53 A GB23333/53 A GB 23333/53A GB 2333353 A GB2333353 A GB 2333353A GB 748715 A GB748715 A GB 748715A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aminoethylamino
- naphthalene
- sulphonic acid
- compounds
- acid
- 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.)
- Expired
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- BOCJQSFSGAZAPQ-UHFFFAOYSA-N 1-chloroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2Cl BOCJQSFSGAZAPQ-UHFFFAOYSA-N 0.000 abstract 2
- GXTWSMPASPGFRQ-UHFFFAOYSA-N 4-[2-(2-aminoethylamino)ethylamino]naphthalene-1-sulfonic acid Chemical compound NCCNCCNC1=CC=C(C2=CC=CC=C12)S(=O)(=O)O GXTWSMPASPGFRQ-UHFFFAOYSA-N 0.000 abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 abstract 2
- 239000000543 intermediate Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- OCIDXARMXNJACB-UHFFFAOYSA-N n'-phenylethane-1,2-diamine Chemical compound NCCNC1=CC=CC=C1 OCIDXARMXNJACB-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 2
- DLKQHBOKULLWDQ-UHFFFAOYSA-N 1-bromonaphthalene Chemical compound C1=CC=C2C(Br)=CC=CC2=C1 DLKQHBOKULLWDQ-UHFFFAOYSA-N 0.000 abstract 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 abstract 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 abstract 1
- -1 aliphatic amines Chemical class 0.000 abstract 1
- 150000004056 anthraquinones Chemical class 0.000 abstract 1
- 125000001769 aryl amino group Chemical group 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 229920002301 cellulose acetate Polymers 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 150000008049 diazo compounds Chemical class 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 238000004043 dyeing Methods 0.000 abstract 1
- 125000004185 ester group Chemical group 0.000 abstract 1
- 125000003106 haloaryl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000002832 nitroso derivatives Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 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
- C09B1/42—Dyes with acylated amino groups the acyl groups being residues of an aromatic carboxylic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/46—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton having the sulfo groups bound to carbon atoms of non-condensed six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/47—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton having at least one of the sulfo groups bound to a carbon atom of a six-membered aromatic ring being part of a condensed ring system
-
- 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
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/28—Dyes with amino groups substituted by hydrocarbon radicals substituted by alkyl, aralkyl or cyclo alkyl groups
- C09B1/285—Dyes with no other substituents than the amino groups
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/918—Cellulose textile
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH748715X | 1952-08-28 | ||
| CH775885X | 1953-07-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB748715A true GB748715A (en) | 1956-05-09 |
Family
ID=25738234
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB23333/53A Expired GB748715A (en) | 1952-08-28 | 1953-08-24 | Manufacture of arylamino-aminoalkyl-compounds |
| GB21329/54A Expired GB775885A (en) | 1952-08-28 | 1954-07-21 | Dyestuff preparations and dyeing or printing processes using them |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB21329/54A Expired GB775885A (en) | 1952-08-28 | 1954-07-21 | Dyestuff preparations and dyeing or printing processes using them |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2888312A (forum.php) |
| BE (1) | BE530577A (forum.php) |
| CH (1) | CH306992A (forum.php) |
| DE (1) | DE932010C (forum.php) |
| FR (1) | FR1105097A (forum.php) |
| GB (2) | GB748715A (forum.php) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1082916B (de) * | 1956-11-07 | 1960-06-09 | Bayer Ag | Verfahren zur Herstellung von N-Anthrachinonyl-aethylendiaminen |
| US3160510A (en) * | 1960-04-25 | 1964-12-08 | Du Pont | Quinacridone pigment compositions |
| NL296822A (forum.php) * | 1960-06-09 | |||
| LU50233A1 (forum.php) * | 1966-01-10 | 1967-07-10 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB428767A (en) * | 1932-10-15 | 1935-05-13 | Chem Ind Basel | Improvements in the dyeing of cellulose acetate artificial silk |
| US2053041A (en) * | 1934-01-27 | 1936-09-01 | Gen Aniline Works Inc | Dyestuff mixture |
| US2150092A (en) * | 1937-02-23 | 1939-03-07 | Du Pont | Process for the preparation of anthraquinonediphenyldithiazoles |
| CH213418A (de) * | 1939-06-10 | 1941-02-15 | Chem Ind Basel | Verfahren zur Herstellung eines Farbstoffpräparates. |
| US2485197A (en) * | 1944-05-24 | 1949-10-18 | Ciba Ltd | Dyestuff mixtures and process of making same |
| US2506020A (en) * | 1947-11-26 | 1950-05-02 | Ciba Ltd | Mixture of insoluble aminoanthraquinone dyes |
| US2768183A (en) * | 1954-08-04 | 1956-10-23 | Gen Aniline & Film Corp | Anthraquinone dyestuffs |
-
0
- BE BE530577D patent/BE530577A/xx unknown
-
1952
- 1952-08-28 CH CH306992D patent/CH306992A/de unknown
-
1953
- 1953-08-24 GB GB23333/53A patent/GB748715A/en not_active Expired
- 1953-08-25 DE DEC8091A patent/DE932010C/de not_active Expired
-
1954
- 1954-07-15 US US443696A patent/US2888312A/en not_active Expired - Lifetime
- 1954-07-21 FR FR1105097D patent/FR1105097A/fr not_active Expired
- 1954-07-21 GB GB21329/54A patent/GB775885A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1105097A (fr) | 1955-11-28 |
| GB775885A (en) | 1957-05-29 |
| DE932010C (de) | 1955-08-22 |
| CH306992A (de) | 1955-05-15 |
| US2888312A (en) | 1959-05-26 |
| BE530577A (forum.php) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2543747A (en) | Preparation of n.n'-diaryl derivatives of perylene diimid | |
| GB748715A (en) | Manufacture of arylamino-aminoalkyl-compounds | |
| US2419405A (en) | Process for preparing 1-hydroxy-4-arylamino anthraquinones | |
| US2006017A (en) | 4-amino-1.8-naphthalene-dicarboxylic acid imides and 4-alkylamino1.8-naphthalene-dicarboxylic acid alkylimides and a process of preparing them | |
| US932290A (en) | Compound of the anthracene series and process of making same. | |
| US2109183A (en) | Process for the manufacture of azo dyestuffs | |
| US2333384A (en) | Arylaminoanthraquinone compound | |
| US2194926A (en) | Mono-nitro-benzene compound and the manufacture thereof | |
| US1874581A (en) | Aromatic monoaroyl diamines | |
| US2132193A (en) | Production of partially hydrogenated hydroxy compounds | |
| US2189367A (en) | Ortho-hydroxycarboxylic acids of the diphenylene series | |
| US2450634A (en) | Production of thiodihydracrylic acids | |
| US1724086A (en) | Eentrich astd max hardtmankt | |
| US2257091A (en) | Solubilization of diazoimino | |
| US1879424A (en) | Watersolttble diazo compound | |
| US2336445A (en) | 4-substituted-2'-substituted diphenyl sulphone | |
| GB731495A (en) | Heterocyclic ether-sulphones | |
| Hauptschein et al. | Trifluoromethylaminosalicylic Acids and Related Reactions1 | |
| US2161524A (en) | Dihydrobenzocarbazole compounds | |
| GB732949A (en) | Monoazo dyestuffs | |
| US1867106A (en) | Hydroxy-benzocarbazole-carboxylic acids | |
| US2705709A (en) | Azo anthraquinone vat dyestuffs | |
| US2443255A (en) | Derivatives of 2-aminc-diphenylsulfone | |
| US2742477A (en) | Amine salts of 2-cyano-naphthalene-1-sulfonic acid | |
| US1787315A (en) | New compounds of the thiazolic series and process of making same |