GB1122389A - Reactive dyestuffs containing a free or salified acid group and a halopyridine residue - Google Patents
Reactive dyestuffs containing a free or salified acid group and a halopyridine residueInfo
- Publication number
- GB1122389A GB1122389A GB3367365A GB3367365A GB1122389A GB 1122389 A GB1122389 A GB 1122389A GB 3367365 A GB3367365 A GB 3367365A GB 3367365 A GB3367365 A GB 3367365A GB 1122389 A GB1122389 A GB 1122389A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- nitro
- pyridine
- salt
- prepared
- 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
- 239000002253 acid Substances 0.000 title abstract 4
- 150000005748 halopyridines Chemical group 0.000 title 1
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 abstract 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 abstract 3
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 abstract 3
- XKWSQIMYNVLGBO-UHFFFAOYSA-N 5-nitro-1h-pyridin-2-one Chemical compound OC1=CC=C([N+]([O-])=O)C=N1 XKWSQIMYNVLGBO-UHFFFAOYSA-N 0.000 abstract 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 2
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 abstract 2
- 235000017550 sodium carbonate Nutrition 0.000 abstract 2
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 2
- DVVGIUUJYPYENY-UHFFFAOYSA-N 1-methylpyridin-2-one Chemical compound CN1C=CC=CC1=O DVVGIUUJYPYENY-UHFFFAOYSA-N 0.000 abstract 1
- OYDCHSBGFDCUGI-UHFFFAOYSA-N 2-chloro-5-nitropyridine-3-sulfonic acid Chemical compound ClC1=NC=C(C=C1S(=O)(=O)O)[N+](=O)[O-] OYDCHSBGFDCUGI-UHFFFAOYSA-N 0.000 abstract 1
- FNUOJWVXAFKPJE-UHFFFAOYSA-N 2-chloro-5-nitropyridine-3-sulfonyl chloride Chemical compound [O-][N+](=O)C1=CN=C(Cl)C(S(Cl)(=O)=O)=C1 FNUOJWVXAFKPJE-UHFFFAOYSA-N 0.000 abstract 1
- IAALHBBKWYRCAF-UHFFFAOYSA-N 2-chloropyridine-3,5-disulfonyl chloride Chemical compound ClS(=O)(=O)C=1C(=NC=C(C1)S(=O)(=O)Cl)Cl IAALHBBKWYRCAF-UHFFFAOYSA-N 0.000 abstract 1
- QXZKKHONVQGXAK-UHFFFAOYSA-N 6-chloropyridine-3-sulfonyl chloride Chemical compound ClC1=CC=C(S(Cl)(=O)=O)C=N1 QXZKKHONVQGXAK-UHFFFAOYSA-N 0.000 abstract 1
- 229910019213 POCl3 Inorganic materials 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 235000010216 calcium carbonate Nutrition 0.000 abstract 1
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract 1
- 150000001805 chlorine compounds Chemical class 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
- 238000006193 diazotization reaction Methods 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 150000002828 nitro derivatives Chemical class 0.000 abstract 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 150000003839 salts Chemical class 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/36—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to some other heterocyclic ring
-
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
- C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
- C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
- C09B29/3617—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom
- C09B29/3621—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring
-
- 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/343—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a five membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR984647A FR1420406A (fr) | 1964-08-08 | 1964-08-08 | Nouveaux colorants réactifs, leurs applications et produits intermédiaires pour leur préparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1122389A true GB1122389A (en) | 1968-08-07 |
Family
ID=8836370
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3367365A Expired GB1122389A (en) | 1964-08-08 | 1965-08-06 | Reactive dyestuffs containing a free or salified acid group and a halopyridine residue |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE667565A (enExample) |
| CH (1) | CH456527A (enExample) |
| DE (1) | DE1469689A1 (enExample) |
| FR (1) | FR1420406A (enExample) |
| GB (1) | GB1122389A (enExample) |
| NL (2) | NL6510350A (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1948354A1 (de) * | 1968-09-24 | 1970-04-23 | Ici Ltd | Reaktivfarbstoffe |
| US4039523A (en) * | 1970-12-22 | 1977-08-02 | Ciba-Geigy Ag | 3-Sulfoalkyl-6-hydroxy-pyrid-(2)-one-containing azo dyestuffs |
| US4092308A (en) * | 1972-10-05 | 1978-05-30 | Ciba-Geigy Corporation | 4-Sulphomethyl substituted hydroxypyridone azo dyestuffs |
| US4213899A (en) * | 1977-05-27 | 1980-07-22 | Imperial Chemical Industries Limited | Reactive dyestuffs containing chlorine or fluorine substituents and one or more pyridine radicals linked to the dyestuff at the 2-, 4- or 6-position |
| US5373094A (en) * | 1992-06-25 | 1994-12-13 | Zeneca Limited | Reactive dyes containing a 2,6-difluoro-3,5-dichloropyridine group |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1350602A (en) * | 1970-07-10 | 1974-04-18 | Ici Ltd | Azo dyestuffs |
| DE19918021C1 (de) | 1999-04-21 | 2000-06-29 | Ruetgers Organics Gmbh | Verfahren zur Herstellung von chlorierten Pyridinsulfonsäurechloriden |
-
0
- NL NL128672D patent/NL128672C/xx active
-
1964
- 1964-08-08 FR FR984647A patent/FR1420406A/fr not_active Expired
-
1965
- 1965-07-23 CH CH1037365A patent/CH456527A/fr unknown
- 1965-07-28 BE BE667565A patent/BE667565A/xx unknown
- 1965-08-04 DE DE19651469689 patent/DE1469689A1/de active Pending
- 1965-08-06 GB GB3367365A patent/GB1122389A/en not_active Expired
- 1965-08-09 NL NL6510350A patent/NL6510350A/xx unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1948354A1 (de) * | 1968-09-24 | 1970-04-23 | Ici Ltd | Reaktivfarbstoffe |
| US4039523A (en) * | 1970-12-22 | 1977-08-02 | Ciba-Geigy Ag | 3-Sulfoalkyl-6-hydroxy-pyrid-(2)-one-containing azo dyestuffs |
| US4092308A (en) * | 1972-10-05 | 1978-05-30 | Ciba-Geigy Corporation | 4-Sulphomethyl substituted hydroxypyridone azo dyestuffs |
| US4213899A (en) * | 1977-05-27 | 1980-07-22 | Imperial Chemical Industries Limited | Reactive dyestuffs containing chlorine or fluorine substituents and one or more pyridine radicals linked to the dyestuff at the 2-, 4- or 6-position |
| US5373094A (en) * | 1992-06-25 | 1994-12-13 | Zeneca Limited | Reactive dyes containing a 2,6-difluoro-3,5-dichloropyridine group |
Also Published As
| Publication number | Publication date |
|---|---|
| BE667565A (enExample) | 1966-01-28 |
| DE1469689A1 (de) | 1968-12-19 |
| NL128672C (enExample) | |
| CH456527A (fr) | 1968-07-31 |
| CH1037365A4 (enExample) | 1968-02-15 |
| NL6510350A (enExample) | 1966-02-09 |
| FR1420406A (fr) | 1965-12-10 |
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