GB612222A - Manufacture of acedianthrone derivatives - Google Patents
Manufacture of acedianthrone derivativesInfo
- Publication number
- GB612222A GB612222A GB1518746A GB1518746A GB612222A GB 612222 A GB612222 A GB 612222A GB 1518746 A GB1518746 A GB 1518746A GB 1518746 A GB1518746 A GB 1518746A GB 612222 A GB612222 A GB 612222A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acedianthrone
- ether
- dichlordimethyl
- reacted
- sulphuric 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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Dye intermediates are made by bromo- or chloro-methylating acedianthrone (see Specification 551,622) or derivatives of acedianthrone containing chloro, bromo, amino, alkoxy, or alkyl substituents in presence of sulphuric acid or aluminium chloride with dichlordimethyl ether or dibromdimethylether (which may be formed in situ from e.g. paraformaldehyde and hydrogen chloride). When aluminium chloride is used, a tertiary base such as pyridine is preferably present, and dichlordimethyl ether may be formed with paraformaldehyde only. In examples, dichlordimethyl ether is reacted in sulphuric acid with (1) acedianthrone, (2) b b 1-dichloracedianthrone, (3) b b 1-dibromoacedianthrone, (4) b b 1-dimethylacedianthrone; also 5) dichlordimethyl ether is reacted with acedianthrone in presence of aluminium chloride and pyridine, and (6) dibromdimethyl ether is reacted with acedianthrone in concentrated sulphuric acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1518746A GB612222A (en) | 1946-05-20 | 1946-05-20 | Manufacture of acedianthrone derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1518746A GB612222A (en) | 1946-05-20 | 1946-05-20 | Manufacture of acedianthrone derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB612222A true GB612222A (en) | 1948-11-10 |
Family
ID=10054547
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1518746A Expired GB612222A (en) | 1946-05-20 | 1946-05-20 | Manufacture of acedianthrone derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB612222A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2645645A (en) * | 1950-12-20 | 1953-07-14 | Gen Aniline & Film Corp | Chloromethylation of arylaminopolycyclic quinones |
US2655515A (en) * | 1950-06-26 | 1953-10-13 | Ici Ltd | Arylaminoacedianthrone isothiouronium salts |
-
1946
- 1946-05-20 GB GB1518746A patent/GB612222A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2655515A (en) * | 1950-06-26 | 1953-10-13 | Ici Ltd | Arylaminoacedianthrone isothiouronium salts |
US2645645A (en) * | 1950-12-20 | 1953-07-14 | Gen Aniline & Film Corp | Chloromethylation of arylaminopolycyclic quinones |
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