HUT37740A - Process for production of phenoxi-alcane acids, their salts and esthers - Google Patents
Process for production of phenoxi-alcane acids, their salts and esthersInfo
- Publication number
- HUT37740A HUT37740A HU220984A HU220984A HUT37740A HU T37740 A HUT37740 A HU T37740A HU 220984 A HU220984 A HU 220984A HU 220984 A HU220984 A HU 220984A HU T37740 A HUT37740 A HU T37740A
- Authority
- HU
- Hungary
- Prior art keywords
- alkali metal
- alkyl
- indicated
- acid
- compsn
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Phenoxy-alkene acids have general compsn. indicated in Fig.(I), X is alkyl gp. or halogen atom which may be replaced by an alkyl halogen gp. having not more than 4 C, n is 0-3, R is H or an alkyl gp. having not more than 3 C. Z is H or alkali metal atom, or an alkyl, alkenyl, alkyl-amine, alkanol, or amine gp., having not more than 10C. In one variant of the method, a phenol cpd. of general compsn. indicated in Fig.(II) where X is as previously stated and m is 0-3, is dissolved in organic solvent immiscible with water and converted into alkali metal salt. In some cases it is reacted with chloralkene acid in presence of phosphorous acid, phosphoric acid or an alkali metal phosphate, and an alkali metal hydroxide, while an azeotropic distillation is carried out. The chlor-alkene acid used has general compsn. indicated in Fig. (III) where R is as before. - In another variant, the phenol cpd. of the general compsn. noted in Fig. (II) where X indicates the chemicals noted in above and m is 0-2, is chlorinated by known method, dissolved in organic solvent immiscible with water and transformed into alkali metal salt. The resulting alkene acid, of general compsn. indicated in Fig. (IV), where R is as before, is chlorinated by known method in presence of phosphor halogenid catalyst with chlor-alkene-acid being obtd. of general compsn. indicated in Fig. (III), reacted in presence of alkali metal hydroxide while carrying out azeotropic distillation
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU220984A HU193574B (en) | 1984-06-08 | 1984-06-08 | Process for production of phenoxialcan acids, their salts and esthers |
GB08514317A GB2162529B (en) | 1984-06-08 | 1985-06-06 | B-cyclodextrin complex of benzene sulphonyl urea derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU220984A HU193574B (en) | 1984-06-08 | 1984-06-08 | Process for production of phenoxialcan acids, their salts and esthers |
Publications (2)
Publication Number | Publication Date |
---|---|
HUT37740A true HUT37740A (en) | 1986-02-28 |
HU193574B HU193574B (en) | 1987-10-28 |
Family
ID=10958304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU220984A HU193574B (en) | 1984-06-08 | 1984-06-08 | Process for production of phenoxialcan acids, their salts and esthers |
Country Status (1)
Country | Link |
---|---|
HU (1) | HU193574B (en) |
-
1984
- 1984-06-08 HU HU220984A patent/HU193574B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
HU193574B (en) | 1987-10-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
HU90 | Patent valid on 900628 | ||
HMM4 | Cancellation of final prot. due to non-payment of fee |