GB668994A - Process for the purification of adrenalin - Google Patents
Process for the purification of adrenalinInfo
- Publication number
- GB668994A GB668994A GB11783/50A GB1178350A GB668994A GB 668994 A GB668994 A GB 668994A GB 11783/50 A GB11783/50 A GB 11783/50A GB 1178350 A GB1178350 A GB 1178350A GB 668994 A GB668994 A GB 668994A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- salts
- arterenol
- ethoxymethylene
- adrenaline
- 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
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/38—Separation; Purification; Stabilisation; Use of additives
- C07C227/40—Separation; Purification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Natural adrenaline is freed from arterenol by contacting an aqueous solution of their acid addition salts with an active methylene compound which may be a lower aliphatic ester of ethoxymethylene - malonic acid, ethoxymethylene-acetoacetic acid, ethoxymethylenecyanoacetic acid, or oxalacetic acid, or acetonylacetone. The reaction is preferably carried out at 75-85 DEG C. in the presence of a water-miscible lower aliphatic alcohol, the active methylene compound being used in 45-50 per cent excess of that required to react with the arterenol present. The mixture is then made alkaline (to pH not above 9.5) when free adrenaline is precipitated. The purification process may be repeated if necessary. The salts of the bases used at the beginning of the process are preferably derived from a weak acid such as acetic, but mineral acid salts may be used. Examples show the use of various methylene compounds, ethyl ethoxymethylenemalonate being preferred. If the product is coloured, it may be treated in acetic acid solution with sodium bisulphite and carbon.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US668994XA | 1949-07-25 | 1949-07-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB668994A true GB668994A (en) | 1952-03-26 |
Family
ID=22072428
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB11783/50A Expired GB668994A (en) | 1949-07-25 | 1950-05-11 | Process for the purification of adrenalin |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB668994A (en) |
-
1950
- 1950-05-11 GB GB11783/50A patent/GB668994A/en not_active Expired
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