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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18182Erstellt: 24. Oktober 2026

Dimethylformamide → 3-Benzyl-7-bromo-5-methyl-benzofuran-2-carbaldehyde

https://huagongshe.com/de/reaction/18182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium HydroxideHCID 14798—
EduktPhosphorus oxychlorideHCID 24813—
Edukt3-Benzyl-7-bromo-5-methyl-benzofuranHCID 59344929—
Produkt3-Benzyl-7-bromo-5-methyl-benzofuran-2-carbaldehydeHCID 5934488961%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

3-Benzyl-7-bromo-5-methyl-benzofuran (3.93 g, 13.05 mmol) was mixed with 10 ml DMF. Phosphorus oxychloride (1.8 ml, 19.3 mmol) was added and the reaction mixture was heated to 50° C. for 16 hours. Additional phosphorus oxychloride (3.6 ml, 38.6 mmol) was added and the reaction mixture was heated to 90° C. for an hour, then to 100° C. for five hours. The mixture was cooled to room temperature, poured onto ice and aqueous sodium hydroxide was added until the mixture reached pH=3. The mixture was extracted with ethyl acetate, dried over magnesium sulfate, filtered, and absorbed onto 20 gm silica gel. The silica gel was layered over 100 gm silica gel in a fritted funnel and eluted with five portions of 400 ml hexanes (to give 0.33 g recovered starting material) and two portions of 400 ml of 10/90 ethyl acetate/hexane to give 3-benzyl-7-bromo-5-methyl-benzofuran-2-carbaldehyde (2.61 g, 61% yield). MS: (M+H)+ 330.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741326B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-8f3be6d1a1a044c5a9bb45c85d9978ee
Quellennotizuspto-grants-2010_06