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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1181339Erstellt: 24. Oktober 2026

Dimethylformamide dimethyl acetal → HCID 58980884, Verbindung

https://huagongshe.com/de/reaction/1181339

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamide dimethyl acetalHCID 78373—
EduktMethyl 3-amino-5-(4-chlorophenyl)thiophene-2-carboxylateHCID 2777492—
Edukt4-(2,2-Diethoxyethoxy)-3-methoxyanilineHCID 11436764—
LösungsmittelEthanolHCID 702—
ProduktHCID 58980884HCID 58980884—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of methyl 3-amino-5-(4-chlorophenyl)-2-thiophenecarboxylate (2.0 g, 7.47 mmol, Maybridge, Inc) in ethanol (20 mL) was added dimethylformamide dimethyl acetal (2.5 mL, 2.5 eq, Aldrich). The reaction mixture was refluxed in a 90° C. oil bath for 3 h at which point the solvents were removed by rotary evaporation. Coevaporation with toluene removed the excess dimethylformamide dimethyl acetal. To the resulting residue was added ethanol (20 mL) and 4-(2,2-diethoxyethoxy)-3-methoxyaniline (2.3 g, 1.2 eq, Example H1). The reaction mixture was heated to 100° C. for 36 hours. The solvent was removed by rotary evaporation and the product purified by column chromatography followed by recrystallization from hot MeOH yielding the intermediate (0.82 g, 22%). 1H NMR (CDCl3) δ 1.22 (6H, t), 3.63-3.83 (4H, m), 3.90 (3H, s), 4.14 (2H, d, J=5.3 Hz), 4.92 (1H, t, J=5.2 Hz), 6.97 (2H), 7.06 (1H, d, J=8.5 Hz), 7.46 (2H, d, J=8.5 Hz), 7.58 (1H, s), 7.68 (2H, d, J=8.4 Hz), 8.24 (1H, br, s). LCMS m/z=501 (m+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07285557B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-5973a2071c764f3f86cac406276b2574
Quellennotizuspto-grants-2007_10