GB764633A - Anthraquinone dyestuff - Google Patents
Anthraquinone dyestuffInfo
- Publication number
- GB764633A GB764633A GB2677/55A GB267755A GB764633A GB 764633 A GB764633 A GB 764633A GB 2677/55 A GB2677/55 A GB 2677/55A GB 267755 A GB267755 A GB 267755A GB 764633 A GB764633 A GB 764633A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cyclohexylamine
- benzyl
- group
- leucoquinizarin
- anthraquinone dyestuff
- 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
- 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
- C09B1/30—Dyes with amino groups substituted by hydrocarbon radicals substituted by alkyl, aralkyl or cyclo alkyl groups sulfonated
- C09B1/306—Dyes with amino groups substituted by hydrocarbon radicals substituted by alkyl, aralkyl or cyclo alkyl groups sulfonated only sulfonated in a substituent
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
4-Benzyl-cyclohexylamine is produced by reacting p-nitrobenzyl chloride with benzene in presence of a Friedel-Crafts catalyst, reducing the nitro group in the p-nitrodiphenylmethane so obtained to amino, and hydrogenating in presence of cobalt oxide.ALSO:The invention comprises a dye for wool of the formula:-<FORM:0764633/IV(b)/1> obtainable by condensing quinizarin or leucoquinizarin with 4-benzyl-cyclohexylamine (see Group IV(b)) and sulphonating. In an example, leucoquinizarin and 4-benzyl-cyclohexylamine are heated together, followed by boiling with nitrobenzene and a little piperidine, and the separated product is sulphonated. Specification 564,859 [Group IV] is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE764633X | 1954-01-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB764633A true GB764633A (en) | 1956-12-28 |
Family
ID=6672902
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2677/55A Expired GB764633A (en) | 1954-01-30 | 1955-01-28 | Anthraquinone dyestuff |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1118335A (en) |
GB (1) | GB764633A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995021813A1 (en) * | 1994-02-10 | 1995-08-17 | John Wyeth & Brother Ltd | Cyclohexane derivatives as voltage-gated potassium channel blockers |
-
1955
- 1955-01-28 FR FR1118335D patent/FR1118335A/en not_active Expired
- 1955-01-28 GB GB2677/55A patent/GB764633A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995021813A1 (en) * | 1994-02-10 | 1995-08-17 | John Wyeth & Brother Ltd | Cyclohexane derivatives as voltage-gated potassium channel blockers |
US5708026A (en) * | 1994-02-10 | 1998-01-13 | John Wyeth & Brother | Cyclohexane derivatives |
AU700058B2 (en) * | 1994-02-10 | 1998-12-17 | John Wyeth & Brother Limited | Cyclohexane derivatives as voltage-gated potassium channel blockers |
Also Published As
Publication number | Publication date |
---|---|
FR1118335A (en) | 1956-06-04 |
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