1,1-Bis(methylthio)-2-nitroethylene → HCID 70537224, Verbindung
Reaktionsgleichung
[CH3:1][S:2][C:3](SC)=[CH:4][N+:5]([O-:7])=[O:6].[NH2:10][CH2:11][CH2:12][CH2:13][O:14][CH2:15][C:16]1[O:20][C:19]([CH2:21][N:22]([CH3:24])[CH3:23])=[CH:18][CH:17]=1>O1CCOCC1>[CH3:24][N:22]([CH3:23])[CH2:21][C:19]1[O:20][C:16]([CH2:15][O:14][CH2:13][CH2:12][CH2:11][NH:10][C:3]([S:2][CH3:1])=[CH:4][N+:5]([O-:7])=[O:6])=[CH:17][CH:18]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of 1,1-bis(methylthio)-2-nitroethene (3.96 g) in dry dioxan (25 ml) at 70° was added dropwise 5-[(3-aminopropoxy)methyl]-N,N-dimethyl-2-furanmethanamine (1.27 g). After 1 hr the reaction was allowed to cool and the solid which separated was filtered. The filtrate and washings were combined and evaporated to dryness, a solution of succinic acid (1 g) in water (25 ml) added to the residue and the suspension filtered. The filtrate was washed with ethyl acetate (2×40 ml) then evaporated to 10 ml. The solution was basified with sodium carbonate and the oily precipitate which separated was extracted into ethyl acetate (3×25 ml). The combined extracts were dried (anhyd. sodium carbonate), the suspension filtered and evaporated to dryness to yield the title compound (1.34 g) as a brown oil.
Aufarbeitung
- temperatureto cool
- customthe solid which separated
- filtrationwas filtered
- customevaporated to dryness
- additiona solution of succinic acid (1 g) in water (25 ml) added to the residue
- filtrationthe suspension filtered
- washThe filtrate was washed with ethyl acetate (2×40 ml)
- customthen evaporated to 10 ml
- customthe oily precipitate which separated
- extractionwas extracted into ethyl acetate (3×25 ml)
- dry with materialThe combined extracts were dried (anhyd. sodium carbonate)
- filtrationthe suspension filtered
- customevaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-13a8e8f86cfa4c22a4b4d432469439d2
- Quelldatensatz
- uspto-grants-1981_12
- Patentnummer
- US04304780
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