GB619658A - Improvements in and relating to the manufacture of organic compounds containing antimony - Google Patents
Improvements in and relating to the manufacture of organic compounds containing antimonyInfo
- Publication number
- GB619658A GB619658A GB3738846A GB3738846A GB619658A GB 619658 A GB619658 A GB 619658A GB 3738846 A GB3738846 A GB 3738846A GB 3738846 A GB3738846 A GB 3738846A GB 619658 A GB619658 A GB 619658A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sodium
- acid
- general formula
- relating
- manufacture
- 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
- 229910052787 antimony Inorganic materials 0.000 title 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000002894 organic compounds Chemical class 0.000 title 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- NLPWTTIYIIOESZ-UHFFFAOYSA-L (4-aminophenyl)stibonic acid Chemical compound NC1=CC=C([Sb](O)(O)=O)C=C1 NLPWTTIYIIOESZ-UHFFFAOYSA-L 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- -1 Organo antimony compounds Chemical class 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 239000012670 alkaline solution Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000002244 precipitate Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- SXYFKXOFMCIXQW-UHFFFAOYSA-N propanedioyl dichloride Chemical class ClC(=O)CC(Cl)=O SXYFKXOFMCIXQW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/90—Antimony compounds
- C07F9/92—Aromatic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
Organo antimony compounds of the general formula <FORM:0619658/IV(b)/1> wherein R and R1 represent hydrogen or alkyl or alkylene radicals (both R and R1 however, not being hydrogen), preferably containing from 1 to 5 and 2 to 5 carbon atoms respectively, are prepared by treating a substituted malonyl chloride with p-aminophenylstibonic acid in aqueous alkaline solution, e.g. by allowing the reactants to remain in contact for at least 24 hours. The product of the reaction may be precipitated as the free acid by the addition of acid, the precipitate redissolved in alkali and the sodium salt precipitated by the addition of alcohol and ether. In examples, the preparation of sodium-diethylmalonyl-, sodium monoethylmalonyl- and sodium diallymalonyl-bis-stibanilates is described. The Provisional Specification refers to a compound of the above general formula in which R and R1 may each represent hydrogen.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3738846A GB619658A (en) | 1946-12-19 | 1946-12-19 | Improvements in and relating to the manufacture of organic compounds containing antimony |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3738846A GB619658A (en) | 1946-12-19 | 1946-12-19 | Improvements in and relating to the manufacture of organic compounds containing antimony |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB619658A true GB619658A (en) | 1949-03-11 |
Family
ID=10396084
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3738846A Expired GB619658A (en) | 1946-12-19 | 1946-12-19 | Improvements in and relating to the manufacture of organic compounds containing antimony |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB619658A (en) |
-
1946
- 1946-12-19 GB GB3738846A patent/GB619658A/en not_active Expired
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