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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 588847Erstellt: 26. Oktober 2026

Dimethylformamide dimethyl acetal → 4,5-Dichloro-2-nitrobenzaldehyde

https://huagongshe.com/reaction/588847

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamide dimethyl acetalHCID 78373—
Edukt1,2-Dichloro-4-methyl-5-nitrobenzeneHCID 343795—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelN,N-Dimethylformamide--water (1/1)HCID 21962138—
Produkt4,5-Dichloro-2-nitrobenzaldehydeHCID 274924623%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A mixture of 1,2-dichloro-4-methyl-5-nitrobenzene (2 g, 9.71 mmol) and DMF-DMA (3 g, 25.2 mmol) in DMF (50 mL) was stirred at 140° C. for 14 h. The dark solution was cooled to 0° C., and then added to a solution of NaIO4 (10.8 g, 50.5 mmol) in DMF/water (1:4, 25 mL) at 0° C. After stirring at room temperature for 8 h, the mixture was filtered and the cake was rinsed with ethyl acetate. The filtrate was diluted with ethyl acetate and washed with brine. The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on silica gel (ethyl acetate/petroleum ether=1:20) to afford the desire product (480 mg, 23% yield, 2 steps)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09227978B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-c85219a211bf4061b3482a5730b3391b
Quellennotizuspto-grants-2016_01