GB362027A - Manufacture of new intermediates for dyes - Google Patents

Manufacture of new intermediates for dyes

Info

Publication number
GB362027A
GB362027A GB2726730A GB2726730A GB362027A GB 362027 A GB362027 A GB 362027A GB 2726730 A GB2726730 A GB 2726730A GB 2726730 A GB2726730 A GB 2726730A GB 362027 A GB362027 A GB 362027A
Authority
GB
United Kingdom
Prior art keywords
aniline
dyes
condensing
nuclear
condensed
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
GB2726730A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to GB2726730A priority Critical patent/GB362027A/en
Publication of GB362027A publication Critical patent/GB362027A/en
Expired legal-status Critical Current

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

Abstract

Arylides of 2 : 3-hydroxynaphthoic acid of the general formula <FORM:0362027/IV/1> where Ar = phenyl or its nuclear alkyloxy, alkyl or halogen substituted derivatives are prepared by condensing o-, m- or p-nitrobenzoic acids or their halides with aniline or its nuclear alkoxy-, alkyl- or halogen substituted derivatives, reducing the nitro group in the resulting product and condensing the aminoaroylamino compounds with 2 : 3 oxynaphthoic acid. They have a pronounced affinity for cotton and yield dyeings of exceptional fastness to light and washing by the ice-colour process. Coupling with diazo compounds in substance yields pigment dyes. In an example, aniline is condensed with p p-nitrobenzoyl chloride in carbon tetrachloride and the product obtained is reduced and condensed with 2 : 3-oxynaphthoic acid; o-anisidine, o-toluidine and 2 : 5-dichloraniline may be used instead of aniline. Specification 23732/13, [Class 2 (iii), Dyes &c.], is referred to.
GB2726730A 1930-09-12 1930-09-12 Manufacture of new intermediates for dyes Expired GB362027A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2726730A GB362027A (en) 1930-09-12 1930-09-12 Manufacture of new intermediates for dyes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2726730A GB362027A (en) 1930-09-12 1930-09-12 Manufacture of new intermediates for dyes

Publications (1)

Publication Number Publication Date
GB362027A true GB362027A (en) 1931-12-03

Family

ID=10256797

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2726730A Expired GB362027A (en) 1930-09-12 1930-09-12 Manufacture of new intermediates for dyes

Country Status (1)

Country Link
GB (1) GB362027A (en)

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