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
GB14175/56A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst AG
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 Hoechst AG, Farbwerke Hoechst AGfiledCriticalHoechst AG
Publication of GB828704ApublicationCriticalpatent/GB828704A/en
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
C09B7/00—Indigoid dyes
C09B7/06—Indone-thionapthene indigos
Landscapes
Chemical & Material Sciences
(AREA)
Organic Chemistry
(AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems
(AREA)
Abstract
4 - Methyl - 5 - bromo - 7 - methoxy - isatin is obtained by sulphonating 4-methyl-7-methoxy-isatin, and reacting the 5-sulphonic acid so obtained in aqueous solution with bromine. It may be converted to its ae-chloride with phosphorus pentachloride.ALSO:The invention comprises a blue-green dye of the formula <FORM:0828704/IV(c)/1> and a method of making it by condensing 4-methyl - 5 - bromo - 7 - methoxy - isatin-a - chloride with 5.7 - dimethyl - 3 - hydroxy-1-thionaphthene. An example is given.
GB14175/56A1955-05-071956-05-07A new vat dyestuff of the indigoid series and process for the manufacture thereof
ExpiredGB828704A
(en)