GB330215A - Improvements in and relating to dyestuff intermediates - Google Patents

Improvements in and relating to dyestuff intermediates

Info

Publication number
GB330215A
GB330215A GB3496028A GB3496028A GB330215A GB 330215 A GB330215 A GB 330215A GB 3496028 A GB3496028 A GB 3496028A GB 3496028 A GB3496028 A GB 3496028A GB 330215 A GB330215 A GB 330215A
Authority
GB
United Kingdom
Prior art keywords
ethers
acid
acetylaminoanthrahydroquinone
acylaminoanthraquinones
chloro
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
GB3496028A
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.)
DAVID ALEXANDER WHYTE FAIRWEAT
Scottish Dyes Ltd
Original Assignee
DAVID ALEXANDER WHYTE FAIRWEAT
Scottish Dyes 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 DAVID ALEXANDER WHYTE FAIRWEAT, Scottish Dyes Ltd filed Critical DAVID ALEXANDER WHYTE FAIRWEAT
Priority to GB3496028A priority Critical patent/GB330215A/en
Publication of GB330215A publication Critical patent/GB330215A/en
Expired legal-status Critical Current

Links

Abstract

330,215. Thomas, J., Fairweather, D. A. W., and Scottish Dyes, Ltd. Nov. 27, 1928. Acylaminoanthraquinones, alkyl ethers of leuco compounds of.-Acylaminoanthraquinones are treated with acid reducing agents, for example, zinc and an acid, preferably acetic acid, and preferably in an alcoholic medium, and the intermediate product thus formed is etherified with or without first isolation to give the 9 : 10-dialkyl ethers of the acylaminoanthrahydroquinones. Alkylation may be effected by means of a dialkylsulphate or a p-toluene sulphonic acid ester, and reduction may take place in an atmosphere of nitrogen as in the examples, which describe the preparation of the 9 : 10-dimethyl ethers of 1- and 2-acetylaminoanthrahydroquinone, 2-benzoylaminoanthrahydroquinone, 1-chloro- and 3-chloro- 2-acetylaminoanthrahydroquinone. The corresponding ethyl and propyl ethers are mentioned. Specification 297,042 is referred to. The Provisional Specification refers to the treatment of vat dyestuffs and intermediates generally.
GB3496028A 1928-11-27 1928-11-27 Improvements in and relating to dyestuff intermediates Expired GB330215A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3496028A GB330215A (en) 1928-11-27 1928-11-27 Improvements in and relating to dyestuff intermediates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3496028A GB330215A (en) 1928-11-27 1928-11-27 Improvements in and relating to dyestuff intermediates

Publications (1)

Publication Number Publication Date
GB330215A true GB330215A (en) 1930-05-27

Family

ID=10372122

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3496028A Expired GB330215A (en) 1928-11-27 1928-11-27 Improvements in and relating to dyestuff intermediates

Country Status (1)

Country Link
GB (1) GB330215A (en)

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