Reaktionsgleichung
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([C:8]#N)=[O:7].Cl.[OH2:11].C.C[OH:14]>>[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6](=[O:7])[C:8]([OH:14])=[O:11]Komponenten
6
Versuchsvorschrift
The 24.5 g. of crude 2-furoylcyanide was mixed with 160 ml. concentrated hydrochloric acid at 25° C. with intermittent stirring. The reaction was stored for 24 hours at 25° C. and diluted with 80 ml. of water. The reaction was stirred for 5 minutes and filtered. The filtrate was saturated with sodium chloride and extracted with 5×120 ml. of 1:1 ether-ethyl acetate solution. The extracts were combined, dried over anhydrous magnesium sulfate and evaporated at 30° C. (15 mm.) to give a brownish-orange solid. The solid was dissolved in methanol, treated with charcoal and evaporated under reduced pressure (15 mm.) to dryness to yield 17 g. of the acid.
Aufarbeitung
- customat 25° C.
- additiondiluted with 80 ml
- filtrationfiltered
- extractionextracted with 5×120 ml
- dry with materialdried over anhydrous magnesium sulfate
- customevaporated at 30° C. (15 mm.)
- customto give a brownish-orange solid
- customevaporated under reduced pressure (15 mm.) to dryness
- customto yield 17 g
Quellen und Nachweise
- ORD-Eintrag
- ord-531f3ac0317542b1a88bbda08ac4d533
- Quelldatensatz
- uspto-grants-1979_12
- Patentnummer
- US04180658
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