AT157108B - Process for the preparation of 5-ethyl- or 5-allyl-5-isobutyl-2-thiobarbituric acids. - Google Patents
Process for the preparation of 5-ethyl- or 5-allyl-5-isobutyl-2-thiobarbituric acids.Info
- Publication number
- AT157108B AT157108B AT157108DA AT157108B AT 157108 B AT157108 B AT 157108B AT 157108D A AT157108D A AT 157108DA AT 157108 B AT157108 B AT 157108B
- Authority
- AT
- Austria
- Prior art keywords
- allyl
- isobutyl
- ethyl
- preparation
- thiobarbituric acids
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung von 5-Äthyl- bzw. 5-Allyl-5-isobutyl-2-thiobarbitursäuren.
Es wurde gefunden, dass man zu den in der Patentschrift Nr. 155904 beschriebenen 5-Äthyl- bzw. 5-Allyl-5-isobutyl-2-thiobarbitursäuren auch in der Weise gelangen kann, dass man in üblicher Weise hergestellten 2-Thiobarbitursäuren, die in 5-Stellung durch einen der angegebenen Reste substituiert sind, nach an sich üblichen Arbeitsweisen, z. B. mit Hilfe umsetzungsfähiger Ester entsprechender Alkohole, beispielsweise mittels der Halogenwasserstoffsäure-, Schwefelsäure-oder Sulfonsäureester, den fehlenden zweiten Rest einführt.
EMI1.1
trockenes Benzol und 8 g Allylbromid werden im Schüttelrohr 4 Stunden auf 1000 erhitzt. Dann saugt man ab, wäscht die Salze mit warmem Benzol nach und verdampft das Benzol.
Der Rückstand aus dem Benzol wird in Essigester gelöst und mit Petroläther die 5-Isobutyl-5-allyl-2-thiobarbitursäure vom F = 146-0 gefällt. Man kann die Umsetzung auch bei Gegenwart eines Katalysators, z. B. etwas Kupferbronze, vornehmen.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Process for the preparation of 5-ethyl- or 5-allyl-5-isobutyl-2-thiobarbituric acids.
It has been found that the 5-ethyl- or 5-allyl-5-isobutyl-2-thiobarbituric acids described in patent specification No. 155904 can also be obtained in such a way that 2-thiobarbituric acids prepared in the usual way, which are substituted in the 5-position by one of the radicals indicated, according to conventional procedures, e.g. B. with the help of reactive esters of corresponding alcohols, for example by means of the hydrohalic acid, sulfuric acid or sulfonic acid ester, introduces the missing second residue.
EMI1.1
dry benzene and 8 g of allyl bromide are heated to 1000 for 4 hours in a shaker tube. It is then filtered off with suction, the salts are washed with warm benzene and the benzene is evaporated.
The residue from the benzene is dissolved in ethyl acetate and 5-isobutyl-5-allyl-2-thiobarbituric acid with a melting point of 146-0 is precipitated with petroleum ether. The reaction can also be carried out in the presence of a catalyst, e.g. B. make some copper bronze.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE157108X | 1935-11-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT157108B true AT157108B (en) | 1939-09-25 |
Family
ID=5678353
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT157108D AT157108B (en) | 1935-11-28 | 1936-11-05 | Process for the preparation of 5-ethyl- or 5-allyl-5-isobutyl-2-thiobarbituric acids. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT157108B (en) |
-
1936
- 1936-11-05 AT AT157108D patent/AT157108B/en active
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