GB430954A - Improvements in the manufacture and production of quinones - Google Patents

Improvements in the manufacture and production of quinones

Info

Publication number
GB430954A
GB430954A GB27920/34A GB2792034A GB430954A GB 430954 A GB430954 A GB 430954A GB 27920/34 A GB27920/34 A GB 27920/34A GB 2792034 A GB2792034 A GB 2792034A GB 430954 A GB430954 A GB 430954A
Authority
GB
United Kingdom
Prior art keywords
quinone
acetic acid
oxide
phenylene oxide
naphthylene
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
GB27920/34A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB430954A publication Critical patent/GB430954A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

<FORM:0430954/IV/1> and derivatives thereof are obtained by treating b -naphthalene phenylene oxide with an oxidizing agent, followed by introducing further substituents, e.g. by nitration, halogenation, or sulphonation. The oxidation may be effected with chromic acid, bichromate in acetic acid, or oxides of nitrogen or air with catalysts. The quinone may be reduced with zinc dust to the b -naphthalenephenylene oxide. The nitrated quinone may be reduced, and the product diazotized, alkylated, aralkylated and acylated. Sulphonating agents produce sulphonic acids, hydroxysulphonic acids, or the hydroxyquinones. Halogen derivatives react with amines to give imides. According to examples, b -naphthylene phenylene oxide is oxidized (1) with chromic anhydride in glacial acetic acid, and (2) in the form of vapour with air over a catalyst of iron vanadate. The Specification as open to inspection under Sect. 91 refers also to the reduction of the quinone to a hydroquinone and the formation of its diacetate, and contains a further example of the oxidation of b -naphthylene phenylene oxide with nitric oxide in acetic acid, with simultaneous formation of a nitration product. This subject-matter does not appear in the Specification as accepted.
GB27920/34A 1933-10-07 1934-09-29 Improvements in the manufacture and production of quinones Expired GB430954A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE430954X 1933-10-07

Publications (1)

Publication Number Publication Date
GB430954A true GB430954A (en) 1935-06-27

Family

ID=6483709

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27920/34A Expired GB430954A (en) 1933-10-07 1934-09-29 Improvements in the manufacture and production of quinones

Country Status (1)

Country Link
GB (1) GB430954A (en)

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