GB1323157A - Waterinsoluble dyestuffs and process for their manufacture - Google Patents
Waterinsoluble dyestuffs and process for their manufactureInfo
- Publication number
- GB1323157A GB1323157A GB3366270A GB3366270A GB1323157A GB 1323157 A GB1323157 A GB 1323157A GB 3366270 A GB3366270 A GB 3366270A GB 3366270 A GB3366270 A GB 3366270A GB 1323157 A GB1323157 A GB 1323157A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compound
- reacting
- prepared
- formula
- amino
- 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
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
- C09B62/04—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 triazine ring
Abstract
1323157 Aniline derivatives CIBA-GEIGY AG 10 July 1970 [11 July 1969] 33662/70 Heading C2C [Also in Division C4] In Preparation I the compound of the formula is prepared by reacting 5-nitro-isophthalic acid chloride with N-ethyl-N-hydroxy-ethyl-m-toluidine, reducing the nitro substituent to amino and then reacting the amino group with trifluorotriazine. In Preparation II, the compound of the formula is prepared by reacting p-nitro-benzoyl chloride with N - ethyl - N - # - hydroxyethyl - m - toluidine, reducing the nitro substituent to amino and then reacting the amino group with trifluorotriazine. The compound of the formula is prepared by a similar method. In Example 8, the compound of the formula is prepared by condensation of p-nitroaniline with cyanoacetic acid to form the compound CN-CH 2 -CONH-C 6 H 5 -NO 2 (p) which is condensed with N,N-di-#-acetoxyethyl-p-aminobenzaldehyde and the product is reduced to convert the nitro substituent to amino.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1066269A CH554402A (en) | 1969-07-11 | 1969-07-11 | PROCESS FOR THE PRODUCTION OF FIBER REACTIVE COLORS. |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1323157A true GB1323157A (en) | 1973-07-11 |
Family
ID=4365515
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3366270A Expired GB1323157A (en) | 1969-07-11 | 1970-07-10 | Waterinsoluble dyestuffs and process for their manufacture |
GB3396172A Expired GB1323158A (en) | 1969-07-11 | 1970-07-10 | Aromatic amines and process for their preparation |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3396172A Expired GB1323158A (en) | 1969-07-11 | 1970-07-10 | Aromatic amines and process for their preparation |
Country Status (7)
Country | Link |
---|---|
BE (1) | BE753292A (en) |
CH (1) | CH554402A (en) |
DE (1) | DE2033253A1 (en) |
FR (1) | FR2054420A5 (en) |
GB (2) | GB1323157A (en) |
NL (1) | NL7010260A (en) |
ZA (1) | ZA704607B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4482490A (en) * | 1979-01-26 | 1984-11-13 | Mitsubishi Chemical Industries, Limited | N-(p-nitrophenyl)-N'-(4-amino-2-fluorotriazineamino phenyl)-1,4-disazophenylene dyes |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3966705A (en) * | 1974-01-04 | 1976-06-29 | Ciba-Geigy Corporation | Disulfo naphthalene containing fiber-reactive tetrazo dyes |
CH614969A5 (en) * | 1975-12-19 | 1979-12-28 | Ciba Geigy Ag | Process for preparing fibre-reactive azo dyes |
CH634093A5 (en) * | 1976-08-02 | 1983-01-14 | Ciba Geigy Ag | Process for preparing fibre-reactive azo dyes |
GB2105738B (en) * | 1981-07-20 | 1985-05-22 | Mitsubishi Chem Ind | Reactive disazo dyes |
DE3320430A1 (en) * | 1983-06-06 | 1984-12-06 | Mitsubishi Chemical Industries Ltd., Tokio/Tokyo | Quinophthalone dyes for cellulose-containing fibres |
-
1969
- 1969-07-11 CH CH1066269A patent/CH554402A/en not_active IP Right Cessation
-
1970
- 1970-07-04 DE DE19702033253 patent/DE2033253A1/en active Pending
- 1970-07-06 ZA ZA704607A patent/ZA704607B/en unknown
- 1970-07-09 FR FR7025543A patent/FR2054420A5/fr not_active Expired
- 1970-07-10 NL NL7010260A patent/NL7010260A/xx unknown
- 1970-07-10 GB GB3366270A patent/GB1323157A/en not_active Expired
- 1970-07-10 BE BE753292D patent/BE753292A/en unknown
- 1970-07-10 GB GB3396172A patent/GB1323158A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4482490A (en) * | 1979-01-26 | 1984-11-13 | Mitsubishi Chemical Industries, Limited | N-(p-nitrophenyl)-N'-(4-amino-2-fluorotriazineamino phenyl)-1,4-disazophenylene dyes |
Also Published As
Publication number | Publication date |
---|---|
FR2054420A5 (en) | 1971-04-16 |
DE2033253A1 (en) | 1971-01-14 |
GB1323158A (en) | 1973-07-11 |
BE753292A (en) | 1971-01-11 |
ZA704607B (en) | 1971-03-31 |
NL7010260A (en) | 1971-01-13 |
CH554402A (en) | 1974-09-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |