AT210413B - Process for the preparation of a new complex compound of 5-nitrofurfural - Google Patents
Process for the preparation of a new complex compound of 5-nitrofurfuralInfo
- Publication number
- AT210413B AT210413B AT613859A AT613859A AT210413B AT 210413 B AT210413 B AT 210413B AT 613859 A AT613859 A AT 613859A AT 613859 A AT613859 A AT 613859A AT 210413 B AT210413 B AT 210413B
- Authority
- AT
- Austria
- Prior art keywords
- nitrofurfural
- preparation
- complex compound
- new complex
- oxazolidone
- Prior art date
Links
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- Plural Heterocyclic Compounds (AREA)
Description
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Verfahren zur Herstellung einer neuen Komplexverbindung des 5-Nitrofurfurols
Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Herstellung einer neuen Komplexverbindung des 5-Nitrofurfurols, welche der Formel :
EMI1.1
EMI1.2
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waschen. Nach dem Trocknen erhält man 23,2 g (=570/0) des Nitrofurfurol-Oxazolidon-Komplexes vom F. 135-140 C. Weitere 13,7 g (=3410) dieser Komplexverbindung erhält man durch Eindampfen des Filtra-
EMI2.1
1110 =Beispiel 2 : a) Eine wässerige Lösung von 1 g des Nitrofurfurol-Oxazolidon-Komplexes wird mit 0, 5 g Semicarbazid-hydrochlorid und 2 Tropfen konz. Salzsäure versetzt und zirka 5 Minuten lang auf 90-100 C erhitzt.
Dann kühlt man auf 2 - 10 C und filtriert das entstandene 5-Nitrofurfurol-semicar- bazon abt F.233 C (Zers. ). Ausbeute : 0, 85 g (=98% d. Th.).
EMI2.2
c) Verwendet man an Stelle des Semicarbazid-hydrochlorids 3-Amino-oxazolidon-(2) und arbeitet sonst in gleicher Weise, wie in Beispiel 2a) beschrieben, so erhält man 0, 9 g (= 91% d. Tb.), N- (5-Nitro- furfuryliden)-3-amino-oxazolidon- (2) von F. 256-2570 C (Zers.).
<Desc / Clms Page number 1>
Process for the preparation of a new complex compound of 5-nitrofurfural
The present invention relates to a process for the preparation of a new complex compound of 5-nitrofurfural which has the formula:
EMI1.1
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to wash. After drying, 23.2 g (= 570/0) of the nitrofurfurol-oxazolidone complex of mp 135-140 ° C. Another 13.7 g (= 3410) of this complex compound are obtained by evaporating the filter
EMI2.1
1110 = Example 2: a) An aqueous solution of 1 g of the nitrofurfurol-oxazolidone complex is concentrated with 0.5 g of semicarbazide hydrochloride and 2 drops. Hydrochloric acid is added and the mixture is heated to 90-100 ° C. for about 5 minutes.
The mixture is then cooled to 2-10 ° C. and the 5-nitrofurfurol-semicar- bazon formed is filtered off at F.233 ° C. (decomp.). Yield: 0.85 g (= 98% of theory).
EMI2.2
c) If you use 3-amino-oxazolidone- (2) instead of the semicarbazide hydrochloride and otherwise work in the same way as described in Example 2a), you get 0.9 g (= 91% of theory), N- (5-nitro-furfurylidene) -3-amino-oxazolidone- (2) of m.p. 256-2570 C (dec.).
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US210413XA | 1958-09-30 | 1958-09-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT210413B true AT210413B (en) | 1960-08-10 |
Family
ID=21801995
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT613859A AT210413B (en) | 1958-09-30 | 1959-08-24 | Process for the preparation of a new complex compound of 5-nitrofurfural |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT210413B (en) |
-
1959
- 1959-08-24 AT AT613859A patent/AT210413B/en active
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