GB403917A - Manufacture of symmetrical di-(arylamino)-hydroxybenzenes - Google Patents
Manufacture of symmetrical di-(arylamino)-hydroxybenzenesInfo
- Publication number
- GB403917A GB403917A GB25100/33A GB2510033A GB403917A GB 403917 A GB403917 A GB 403917A GB 25100/33 A GB25100/33 A GB 25100/33A GB 2510033 A GB2510033 A GB 2510033A GB 403917 A GB403917 A GB 403917A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxybenzenes
- arylamino
- symmetrical
- manufacture
- reaction
- 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
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/74—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C215/76—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton of the same non-condensed six-membered aromatic ring
- C07C215/82—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the amino groups further bound to a carbon atom of another six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Symmetrical di-(arylamino)-hydroxybenzenes are manufactured by heating one molecular proportion of phloroglucinol with about two molecular proportions of an aromatic amine, if necessary in the presence of a diluent, e.g. xylene, at about 140 DEG C. in such a manner that the water formed during the reaction distils from the reaction mixture. The products are intermediates for the manufacture of dyestuffs. Examples describe the reaction of phloroglucinol with p-chloraniline, aniline, o-and p-toluidine, p-anisidine, m-xylidine (CH3 : CH3 : NH2=1 : 3 : 4), b -naphthylamine and m-nitraniline. In the last case a small quantity of the monoarylaminodihydroxybenzene is obtained as a by-product.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE403917X | 1932-09-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB403917A true GB403917A (en) | 1934-01-04 |
Family
ID=6419856
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB25100/33A Expired GB403917A (en) | 1932-09-09 | 1933-09-11 | Manufacture of symmetrical di-(arylamino)-hydroxybenzenes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB403917A (en) |
-
1933
- 1933-09-11 GB GB25100/33A patent/GB403917A/en not_active Expired
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