GB501131A - Manufacture of new azo dyestuffs - Google Patents

Manufacture of new azo dyestuffs

Info

Publication number
GB501131A
GB501131A GB1957137A GB1957137A GB501131A GB 501131 A GB501131 A GB 501131A GB 1957137 A GB1957137 A GB 1957137A GB 1957137 A GB1957137 A GB 1957137A GB 501131 A GB501131 A GB 501131A
Authority
GB
United Kingdom
Prior art keywords
naphthol
acid
benzylaniline
nitro
sulphonic
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
Application number
GB1957137A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
WILFRID HERBERT CLIFFE
Imperial Chemical Industries Ltd
Original Assignee
WILFRID HERBERT CLIFFE
Imperial Chemical Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by WILFRID HERBERT CLIFFE, Imperial Chemical Industries Ltd filed Critical WILFRID HERBERT CLIFFE
Priority to GB1957137A priority Critical patent/GB501131A/en
Publication of GB501131A publication Critical patent/GB501131A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/02Disazo dyes
    • C09B35/039Disazo dyes characterised by the tetrazo component
    • C09B35/28Disazo dyes characterised by the tetrazo component the tetrazo component containing two aryl nuclei linked by at least one of the groups —CON<, —SO2N<, —SO2—, or —SO2—O—

Abstract

501,131. Dyes. CLIFFE, W. H., and IMPERIAL CHEMICAL INDUSTRIES, Ltd. July 14, 1937, No. 19571. Samples furnished. (Class 2 (iii)] Disazo dyestuffs, containing sufficient sulphonic acid, sulphuric ester or other solubilizing groups to ensure their being soluble in water, are manufactured by tetrazotizing a diaminobenzoylaniline of the general formula in which R is an aralkyl group or a hydroxyalkyl group or sulphuric ester thereof, an alkoxyalkyl group or an acetoxyalkyl group, the alkyl radicle being ethyl, propyl or butyl, and in which either or both of the phenylene radicles may contain one or more substituents including short chain alkyl groups, and coupling with two molecular proportions of the same or different coupling components, e.g. phenols, naphthols, naphtholsulphonic acids, naphthylamines, naphthylaminesulphonic acids, aminonaphthols- or their sulphonic acids or N-substituted derivatives, arylpyrazolones or sulphonic or carboxylic acids thereof or acetoacetic arylamides. Alternatively, there may be employed a compound having the general formula given above except that one or other (but not both), of the amino groups is replaced by a'nitro group, this compound being diazotized and coupled with one molecular proportion of a coupling component, the nitro group then being reduced and the product diazotized and coupled with one molecular proportion of the same or a different coupling component. When R is a hydroxyalkyl group, the products may be subsequently converted to their sulphuric esters, e.g. by treatment with 80 per cent sulphuric acid. The products dye wool from a neutral or acid bath. In examples : (1) 3 : 3<1>diaminobenzoyl-N-#-hydroxyethylaniline is tetrazotized and coupled with two molecular proportions of 1-(4<1>-sulphophenyl-3-methyl-5-pyrazolone; the product dyes wool yellow shades; (2) the product of (1) is treated with concentrated sulphuric acid (similar shades); (3) the coupling component in (1) is replaced by 2-phenylamino- 8-naphthol-6-sulphonic acid; (4) 3 3<1>-diamino- 6<1>-methylbenzoyl - N - benzylanine is tetrazotized and coupled with two molecular proportions of 1-acetylamino-8-naphthol-3: 6-disulphonic acid (bluish-red shades); (5) the coupling component in (4) is replaced by 2-naphthol- 6: 8-disulphonic acid (orange shades); and (6) by 2-acetylamino-8-naphthol-6-sulphonic acid (scarlet shades); (7) 4: 3<1>-diaminobenzoyl-N- benzylaniline is tetrazotized and coupled with two molecular proportions of 2-naphthol-6 : 8-. disulphonic acid (orange shades); (8) 3: 4<1> diamino - 4 - methylbenzoyl -N - benzylanilide is tetrazotized and coupled with two molecular proportions of 1-(4<1>-sulphophenyl)-3-methyl-5- pyrazolone (yellow shades). A table gives the shades of further dyestuffs, the following additional coupling components being specified: 1-(2<1> : 5<1>-dichloro-4<1>-sulphophenyl)-3-methyl-5- pyrazolone, 2 - naphthol - 8 - sulphonic acid, 2- acetylamino - 5 - naphthol - 7 - sulphonic acid, 1- naphthol - 4 - sulplionic acid, 2 - N - # - hydroxyethylamino- 8 -naphthol- 6 -sulphonic acid and 1 - benzoylamino - 8 - naphthol - 4 : 6 - diswphonic acid. Diamino- or nitroaminobenzoyl-N-aralkylhydroxyalkyl- or -alkoxyalkylanilines are obtainable by condensing a mononitro-N-aralkyl-, hydroxyalkyl- or -alkoxyalkylarylamine of the benzene series with a nitroaroyl chloride of the benzene series and reducing one or both nitro groups. In examples: (1) N-#-hydroxyethylm-nitraniline is heated with m-nitrobenzoyl chloride, and the product is reduced with iron and hydrochloric acid in water or ethyl alcohol to 3 : 3<1> - diaminobenzoyl - N - # - hydroxyethylaniline ; (4) 2 - benzylamino - 4 - nitrotoluene similarly yields 3 : 3<1>-diamino-6<1>-methylbenzoyl- N-benzylaniline; (7) 3-nitro-N-benzylaniline and p-nitrobenzoyl chloride similarly yield 4 : 3<1> - diaminobenzoyl - N - benzylaniline; (8) 4-nitro-N-benzylaniline and 3-nitro-4-methylbenzoyl chloride similarly yield 3 : 4<1>-diamino-4- methylbenzoyl-N-benzylaniline. Diumino- or nitroaminobenzoyl-N-acetoxyalkylanilines are obtainable by condensing a mononitro - N - hydroxyalkylarylamine with a nitroaroyl chloride, heating the product with acetic anhydride and reducing one or both nitro groups. Samples have been furnished under Sect. 2 (5) of the following dyestuffs : (A) 2-naphthol-8- sulphonic acid # 3: 3<1>-diamino-6<1>-methylbenzoyl-N-benzylaniline # 1-naphthol-4-sulphonic acid; (B) 3:3<1>-diaminobenzoyl-N-#- ethoxyethylaniline (obtainable by condensing m-nitraniline with #-ethoxyethyl p-toluenesulphonate, condensing the produqt with m-nitrobenzoyl chloride and reducing) <#>#2-acetylamino-8-naphthol-6-sulphonic acid (2 mols.); (C) 3:3<1>-diaminobenzoyl-N-#-acetoxyethylaniline (obtainable by treating 3 : 3<1>-dinitro beuzoyl-N-#-hydroxyethylaniline with glacial acetic acid and-acetic anhydride in the presence of sodium acetate, and reducing)<#># 2-naphthol- 6: 8-disulphonic acid (2 mols.); (D) 1-naphthol- 4 -sulphonic. acid # 3<1>- nitro 4 - amino -6<1>- methylbenzoyl-N-benzylaniline (obtainable by condensing 2-benzylamino-4-nitrotoluene with p-nitrobenzoyl chloride and reducing one nitro group) (reduced) # 2-naphthol-6: 8-disulphonic acid.
GB1957137A 1937-07-14 1937-07-14 Manufacture of new azo dyestuffs Expired GB501131A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1957137A GB501131A (en) 1937-07-14 1937-07-14 Manufacture of new azo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1957137A GB501131A (en) 1937-07-14 1937-07-14 Manufacture of new azo dyestuffs

Publications (1)

Publication Number Publication Date
GB501131A true GB501131A (en) 1939-02-14

Family

ID=10131592

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1957137A Expired GB501131A (en) 1937-07-14 1937-07-14 Manufacture of new azo dyestuffs

Country Status (1)

Country Link
GB (1) GB501131A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2448853A (en) * 1945-12-29 1948-09-07 Eastman Kodak Co Sulfonamido disazo dye

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2448853A (en) * 1945-12-29 1948-09-07 Eastman Kodak Co Sulfonamido disazo dye

Similar Documents

Publication Publication Date Title
US2194927A (en) Azo compound
US2384419A (en) Azo dyestuffs
GB501131A (en) Manufacture of new azo dyestuffs
US2195788A (en) Complex metal compoijnds of azo
US2196028A (en) Azo dyestuffs
US2157877A (en) Polyazo dyestuffs
US2216229A (en) Manufacture of new azo dyestuffs
US1901387A (en) Azodyestuffs
US2556743A (en) Metallized azo dyes
US2248151A (en) Production of substantive azo dyestuffs
US2152408A (en) Secondary disazo dyestuffs
US2200414A (en) Manufacture of new azo dyestuffs
US2095484A (en) Azodyestuffs
US1913384A (en) Trisazo dyestuff and process of preparing the same
US2034247A (en) Azo dyestuffs
US2181051A (en) Monoazo dyestuffs
US2650916A (en) Disazo dyestuffs
US2342451A (en) Chrome disazo dye
US2982764A (en) Copper-containing trisazo dyestuffs
US2028439A (en) Disazodyestuffs
US2163251A (en) Azo dyestuffs
US4137228A (en) Water-soluble, copper containing trisazo compounds having a 2-(4&#39;phenylene)-benzimidazoyl-(5 or 6),-benzoxazolyl-(5), or -benzthiazolyl-(5) component
US2495243A (en) Esterlike derivatives of azo dyestuffs
US1686947A (en) Diazotizable azodyestuffs
US1871991A (en) New azo dyestuffs