DE473151C - Process for obtaining total alkaloids from ergot - Google Patents
Process for obtaining total alkaloids from ergotInfo
- Publication number
- DE473151C DE473151C DEST40748D DEST040748D DE473151C DE 473151 C DE473151 C DE 473151C DE ST40748 D DEST40748 D DE ST40748D DE ST040748 D DEST040748 D DE ST040748D DE 473151 C DE473151 C DE 473151C
- Authority
- DE
- Germany
- Prior art keywords
- ergot
- alkaloids
- total alkaloids
- obtaining total
- alcohol
- 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
- C07G—COMPOUNDS OF UNKNOWN CONSTITUTION
- C07G5/00—Alkaloids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
Verfahren zur Gewinnung der Gesamtalkaloide aus 1Kutterkorn Durch das Hauptpatent 439 042 ist ein Verfahren geschützt, mit -dessen Hilfe es möglich ist, die Alkaloide aus dem Mutterkorn ohne die sonst übliche vorherige Entfettung herauszulösen und in- einem Arbeitsgange fettfrei zu gewinnen.Process for obtaining the total alkaloids from 1Kutterkorn Avg the main patent 439 042 is a process protected, with the help of which it is possible is, the alkaloids from ergot without the usual prior degreasing to be extracted and to be extracted fat-free in one operation.
Es wurde nun festgestellt, daB es möglich ist, das im Hauptpatent verwendete Aceton durch 45- bis 6oprozentigen Äthylalkohol zu ersetzen und mit diesem Lösungsmittel ein gleich günstiges Ergebnis zu erzielen. Im übrigen wird dasVerfahren in analogerWeise wie dasjenige des Hauptpatentes durchgeführt.It has now been found that it is possible to do so in the main patent used to replace acetone with 45 to 6 percent ethyl alcohol and with this Solvent to achieve an equally favorable result. Otherwise the procedure is carried out in a manner analogous to that of the main patent.
Alkohol der angegebenen Konzentration wurde bis jetzt nur zur Gewinnung von Mutterkornextrakten, nicht aber zur Abscheidung der Alkaloide verwendet. Die älteren Untersucher haben aber die Bedeutung, welche die Löslichkeit der Alkaloide in verdünntem Alkohol für die Abscheidung besitzt, nicht erkannt, sondern im Gegenteil diejenigen Stoffe, welche bei der Entfernung oder Verdünnung des Alkohols ausfallen, entfernt und das Filtrat zur Gewinnung des Extraktes weiterverarbeitet. Bei dieser Arbeitsweise gehen aber erhebliche Mengen der Alkaloide verloren, die nach dem neuen Verfahren gewonnen werden.Alcohol of the stated concentration has only been used for extraction until now from ergot extracts, but not used to separate the alkaloids. the but older investigators have the importance of the solubility of the alkaloids possesses in dilute alcohol for the deposition, not recognized, but on the contrary those substances which precipitate when the alcohol is removed or diluted, removed and the filtrate processed to obtain the extract. At this However, considerable amounts of the alkaloids are lost after the new one works Procedure can be obtained.
Beispiel i kg gemahlenes Mutterkorn wird mit 2i', Liter einer Mischung von gleichen Teilen Alkohol und Wasser pereoliert.Example 1 kg of ground ergot is mixed with 2½ liters pereolated from equal parts of alcohol and water.
Das fettfreie Percolat reagiert stark sauer. Durch allmählich erfolgenden Zusatz von 40 bis 5o ccm ioprozentiger Natronlauge wird die Säure so weit abgestumpft, daß nach dreistündigem Stehen eine nur ganz schwach saure Reaktion bestehen bleibt.The fat-free percolate reacts strongly acidic. By gradually occurring The addition of 40 to 50 ccm of 10% sodium hydroxide solution will dull the acid to such an extent that that after standing for three hours a very weakly acidic reaction persists.
Aus dem Percolat wird der Alkohol durch Destillation im Vakuum bei niederer Temperatur verjagt. Hierbei scheidet sich ein in Wasser unlöslicher, hellbrauner, flockiger Niederschlag aus, der die gesamten Alkaloide enthält. Er wird abfiltriert, ausgewaschen und getrocknet. Ausbeute an Rohalkaloid 7e2 g.The alcohol is expelled from the percolate by distillation in vacuo at a low temperature. A light brown, flaky precipitate, which is insoluble in water and contains all of the alkaloids, separates out. It is filtered off, washed and dried. Yield of crude alkaloid 7e2 g.
Das so gewonnene Rohprodukt kann nach den bekannten Alkaloidreinigungsmethoden in reines Alkaloidpräparat übergeführt werden. Ausbeute ungefähr o,8 g.The crude product obtained in this way can be purified by the known alkaloid cleaning methods be converted into a pure alkaloid preparation. Yield about 0.8 g.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEST40748D DE473151C (en) | 1926-03-18 | 1926-03-18 | Process for obtaining total alkaloids from ergot |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEST40748D DE473151C (en) | 1926-03-18 | 1926-03-18 | Process for obtaining total alkaloids from ergot |
Publications (1)
Publication Number | Publication Date |
---|---|
DE473151C true DE473151C (en) | 1929-03-11 |
Family
ID=7463791
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEST40748D Expired DE473151C (en) | 1926-03-18 | 1926-03-18 | Process for obtaining total alkaloids from ergot |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE473151C (en) |
-
1926
- 1926-03-18 DE DEST40748D patent/DE473151C/en not_active Expired
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