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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1246634Erstellt: 26. Oktober 2026

Dimethylformamide → 3-Chloro-5-methoxybenzaldehyde

https://huagongshe.com/reaction/1246634

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktEthyl AcetateHCID 8857—
Edukt3,5-DichloroanisoleHCID 36588—
EduktMagnesiumHCID 5462224—
Katalysator1,2-DibromoethaneHCID 7839—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Chloro-5-methoxybenzaldehydeHCID 2190463354%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3,5-Dichloroanisole (74.0 g, 419 mmol) in THF (200 mL) was added dropwise to magnesium metal (14.2 g, 585 mmol, pre-washed with 0.5 N HCl) in THF (100 mL) at 25° C. After the addition, 1,2-dibromoethane (3.9 g, 20.8 mmol) was added dropwise. The resultant dark brown mixture was heated at reflux for 3 h. The mixture was cooled to 0° C., and N,N-dimethylformamide (60 mL) was added in one portion. The mixture was partitioned with diethyl ether (3×400 mL) and 6N HCl (500 mL). The combined organic extracts were washed with brine (300 mL), dried (Na2SO4), filtered and concentrated in vacuo to give an oil. Flash chromatography (2×) on silica gel eluting with Hex:EtOAc (4:1) afforded the sub-title compound (38.9 g, 54%/) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07129233B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-3c16a7f0c46742808877c6222350da3d
Quellennotizuspto-grants-2006_10