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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1373692Erstellt: 26. Oktober 2026

Dimethylformamide → 2-Bromo-4-(bromomethyl)benzaldehyde

https://huagongshe.com/reaction/1373692

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPhosphorus oxybromideHCID 24613—
EduktSodium BicarbonateHCID 516892—
Edukt2-Bromo-4-(hydroxymethyl)benzaldehydeHCID 18374372—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Bromo-4-(bromomethyl)benzaldehydeHCID 12016038113,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirring cold (0° C.) solution of POBr3 (0.6 mol, 171 g) in CH2Cl2 (1.6 L) was added dropwise DMF (0.75 L) over a period of 1 h. A solution of 2-bromo-4-hydroxymethyl-benzaldehyde (0.49 mol, 107 g) in CH2Cl2 (0.75 L) was then added dropwise over a period of 0.5 h. The resulting mixture was stirred at 0° C. for another 0.5 h and was then transferred via a cannula to a cold (0° C.) stirring aqueous solution of NaHCO3 (3 L, 1M) while maintaining the temperature of the aqueous solution below 10° C. After the transfer was completed, the mixture was extracted with CH2Cl2 (2 L). The organic extract was separated and washed with H2O (3 L) and brine (3 L), dried with MgSO4 (anhyd.) and concentrated to give an oil . The residue was extracted with 10% EtOAc/hexane (2 L). The organic extract was washed with H2O (2×1 L), dried with MgSO4 (anhyd.) and concentrated to a solid which was swished with hexane to give 154 g (˜100%) of the title compound as a beige solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07163932B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-0bd9025d21bc48a48f6af550443f2cde
Quellennotizuspto-grants-2007_01