GB316143A - Process for the manufacture of hydroxy-1. 8-naphthoylene-naphthimidazoles and sulphuric acids thereof - Google Patents
Process for the manufacture of hydroxy-1. 8-naphthoylene-naphthimidazoles and sulphuric acids thereofInfo
- Publication number
- GB316143A GB316143A GB22492/29A GB2249229A GB316143A GB 316143 A GB316143 A GB 316143A GB 22492/29 A GB22492/29 A GB 22492/29A GB 2249229 A GB2249229 A GB 2249229A GB 316143 A GB316143 A GB 316143A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxy
- naphthoylene
- sulphonic
- naphthimidazole
- acid
- 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
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/12—Perinones, i.e. naphthoylene-aryl-imidazoles
Abstract
316,143. I. G. Farbenindustrie Akt.- Ges. July 23, 1928, [Convention date]. Hydroxy - 1<1> : 8' naphthoylenenaphthimidazoles, and sulphonic acids thereof are made by fusing with caustic alkali a 1<1> : 8<1>-naphtheylenenaphthimidazole sulphonic acid obtainable by condensing naphthalic acid anhydride with an onaphthylenediamine mono- or polysulphonic acid. In examples (1) 1<1> : 8<1>-naphthoylene-a-1 : 2- naphthimidazole-6- or 8-sulphonic acid (from 1 : 2-naphthylenediarnine-5- or 7-sulphonic acid respectively and naphthalic anhydride) is fused with caustic potash to form the 6- or 8-hydroxy compound respectively, (2) 1<1> : 8<1>-naphthoylenea-1 : 2-naphthimidazole-6 : 8- or 7 : 9-disulphonic acid (obtained from 1 : : 2-naphthylenediamine- 5: 7- and 6 : 8-disulphonic acid respectively and naphthalic anhydride) is fused with caustic potash to form 1<1> : 8<1>-naphthoylene-a-1 : 2- naphthimidazole - 6 - hydroxy-8-sulphonic or 9- hydroxy-7-sulphonic acid respectively. The Specification as open to inspection under Sect, 91 (3) (a) states that 6-hydroxy-3<1> or 6<1>- hydroxy - 1<1> : 8<1> - naphthoylene-a-1 : 2-naphthimidazole, and 6-hydroxy-4<1>- or 5<1>-hydroxy-1<1> : 8<1>- naphthoylene-a-1 : 2-naphthimidazole may be obtained in a similar manner. It also states that derivatives of hydroxy-1<1> : 8<1>-naphthoylenenaphthimidazoles and their sulphonic acids may be obtained from derivatives of 1<1> : 8<1>- naphthoylenenaphthimidazole sulphonic acids and derivatives of naphthalic anhydride. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE316143X | 1928-07-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB316143A true GB316143A (en) | 1930-08-28 |
Family
ID=6150399
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB22492/29A Expired GB316143A (en) | 1928-07-23 | 1929-07-22 | Process for the manufacture of hydroxy-1. 8-naphthoylene-naphthimidazoles and sulphuric acids thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB316143A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4097450A (en) * | 1976-09-14 | 1978-06-27 | Hoechst Aktiengesellschaft | Perinone compounds as colorants for polyolefins |
-
1929
- 1929-07-22 GB GB22492/29A patent/GB316143A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4097450A (en) * | 1976-09-14 | 1978-06-27 | Hoechst Aktiengesellschaft | Perinone compounds as colorants for polyolefins |
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