CH299273A - Process for the production of a thiosemicarbazone. - Google Patents
Process for the production of a thiosemicarbazone.Info
- Publication number
- CH299273A CH299273A CH299273DA CH299273A CH 299273 A CH299273 A CH 299273A CH 299273D A CH299273D A CH 299273DA CH 299273 A CH299273 A CH 299273A
- Authority
- CH
- Switzerland
- Prior art keywords
- thiosemicarbazone
- production
- benzaldehyde
- butylsulfone
- reacted
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Thiosernicarbazons. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines Thio- semicarbazons, das dadurch gekennzeichnet ist, dass man Benzaldehyd-4-n-butyl-sulfon mit Thiosemicarbazid umsetzt und das ent sprechende Thiosemicarbazon rein gewinnt.
Die neue Verbindung kann ausser zur Bekämpfung von Tuberkuloseinfektionen auch zu andern Zwecken, z. B. zur Schädlings bekämpfung, Verwendung finden. <I>Beispiel:</I> 22 g Benzaldehyd-4-n-butylsulfon werden in 100 cms heissem Alkohol gelöst und mit einer heissen Lösung von 10 g Thiosemicarb- azid in 100 cm3 Wasser versetzt. Nach Zu gabe von 5 cm3 Eisessig wird 30 Minuten ge- kocht und abgekühlt. Das auskristallisierte Thiosemicarbazon wird aus Alkohol umkri stallisiert.
Man erhält das Benzaldehyd-4-n- butyl - sulfon - thiosemicarbazon in schwach gelblich gefärbten Kristallen vom Schmelz punkt 194 C.
Process for the production of a thiosernicarbazone. The present patent relates to a process for the production of a thiosemicarbazone which is characterized in that benzaldehyde-4-n-butyl-sulfone is reacted with thiosemicarbazide and the corresponding thiosemicarbazone is obtained in pure form.
In addition to combating tuberculosis infections, the new compound can also be used for other purposes, e.g. B. for pest control, use. <I> Example: </I> 22 g of benzaldehyde-4-n-butylsulfone are dissolved in 100 cms of hot alcohol and a hot solution of 10 g of thiosemicarbazide in 100 cm3 of water is added. After adding 5 cm3 of glacial acetic acid, the mixture is boiled for 30 minutes and then cooled. The crystallized thiosemicarbazone is crystallized from alcohol.
Benzaldehyde-4-n-butyl-sulfone-thiosemicarbazone is obtained in pale yellowish crystals with a melting point of 194 C.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE299273X | 1944-12-22 | ||
CH296183T | 1951-06-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH299273A true CH299273A (en) | 1954-05-31 |
Family
ID=25733673
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH299273D CH299273A (en) | 1944-12-22 | 1951-06-26 | Process for the production of a thiosemicarbazone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH299273A (en) |
-
1951
- 1951-06-26 CH CH299273D patent/CH299273A/en unknown
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