Diethyl Ether → HCID 178522917, Verbindung

Reaktionsgleichung

[F:1][C:2]1[CH:8]=[C:7]([I:9])[CH:6]=[CH:5][C:3]=1[NH2:4].[C:10]1(=[O:24])OC(OC(CC)(CC)C)[O:14][C:12](=O)[CH2:11]1.[Cl:25][C:26]1[CH:33]=[CH:32][C:29]([CH2:30][NH2:31])=[CH:28][CH:27]=1.[CH2:34](OCC)C>>[Cl:25][C:26]1[CH:33]=[CH:32][C:29]([CH2:30][NH:31][C:10]([C:11]2[CH:34]=[N:4][C:3]3[C:5]([C:12]=2[OH:14])=[CH:6][C:7]([I:9])=[CH:8][C:2]=3[F:1])=[O:24])=[CH:28][CH:27]=1

Komponenten

Edukt 4

HCID 3283Diethyl Ether

HCID 660364-Chlorobenzylamine

HCID 1856942-Fluoro-4-iodoaniline

HCID 131717023Diethylethoxymethylene malonate

Produkt 1

HCID 178522917HCID 178522917, Verbindung

Reaktionsbedingungen

Temperatur: 130 °C

Versuchsvorschrift

A mixture of 11.85 g of 2-fluoro-4-iodoaniline and 10.81 g of diethylethoxymethylene malonate is heated to 130° C. in a flask equipped with a Dean-Stark trap to collect formed ethanol. The mixture is then cooled to 75° C. and diluted with hexanes. The resulting solid is collected and dried. The solid is then dissolved in 60 mL diphenyl ether and heated to 250° C. for 3 h in a flask equipped with a Dean-Stark trap to collect the ethanol. The solution is allowed to cool to room temperature and the resulting solid is collected and dried to yield 11.73 g. This material(0.55 g) and 3 mL of 4-chlorobenzylamine are heated at 180° C. for 1 h. The reaction is cooled and poured into 75 mL diethyl ether. The resulting solid is filtered and recrystallized from ethyl acetate/hexanes to give the title compound as an off-white solid (0.45 g).