GB263845A - Manufacture of benzanthrone derivatives - Google Patents
Manufacture of benzanthrone derivativesInfo
- Publication number
- GB263845A GB263845A GB32841/26A GB3284126A GB263845A GB 263845 A GB263845 A GB 263845A GB 32841/26 A GB32841/26 A GB 32841/26A GB 3284126 A GB3284126 A GB 3284126A GB 263845 A GB263845 A GB 263845A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxy
- acid
- oxybenzanthrone
- aroyloxybenzanthrones
- methylated
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/26—Quinones containing groups having oxygen atoms singly bound to carbon atoms
- C07C50/36—Quinones containing groups having oxygen atoms singly bound to carbon atoms the quinoid structure being part of a condensed ring system having four or more rings
-
- 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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/50—Dibenzopyrenequinones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
263,845. I. G. Farbenindustrie Akt.- Ges. Dec. 30, 1925, [Convention date]. Addition to 248,791. Oxy and alkyloxy-dibenzpyrenequinones.-Bz2- Aroyloxybenzanthrones are treated with acid condensing agents. The oxydibenzpyrenequinones so obtained dye cotton from the vat in reddish-brown shades not fast to acid; by alkylation they yield products which dye in fast yellow shades. According to examples (1) Bz 2-benzoyloxybenzanthrone is heated with a mixture of aluminium and sodium chlorides and the 1-oxy- 3:4:8: 9-dibenzpyrenequinone methylated or ethylated with p-toluenesulphonic methyl or ethyl ester in nitrobenzene; (2) the p-taluic ester of Bz2-oxybenzanthrone is similarly treated and the 1 - oxy-3 : 4-methylbenz - 8: 9-benzpyrenequinone methylated. Bz2-Benzoyl and p-toluoyl-oxybenzanthrones are obtained from Bz2-oxybenzanthrone bv benzoylation by the Schotten-Baumann method, and by heating with p-toluic acid chloride respectively. The Specification as open to inspection under Sect. 91 (3) (a) refers to the treatment with acid condensing agents of substitution products of Bz2- aroyloxybenzanthrones which possess free peripositions in the naphthalene nucleus. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE263845X | 1925-12-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB263845A true GB263845A (en) | 1927-09-29 |
Family
ID=5986440
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32841/26A Expired GB263845A (en) | 1925-12-30 | 1926-12-29 | Manufacture of benzanthrone derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB263845A (en) |
-
1926
- 1926-12-29 GB GB32841/26A patent/GB263845A/en not_active Expired
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