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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2175Erstellt: 23. Oktober 2026

Dimethylformamide → 2-(4-Chlorophenyl)-3-(dimethylamino)acrylaldehyde

https://huagongshe.com/de/reaction/2175

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt(4-Chlorophenyl)acetic acidHCID 15880—
EduktPhosphorus oxychlorideHCID 24813—
LösungsmittelTolueneHCID 1140—
Produkt2-(4-Chlorophenyl)-3-(dimethylamino)acrylaldehydeHCID 3448972—

Reaktionsschritte

Phosphorus oxychloride (92 g) was added dropwise to stirred DMF (78 ml) between 10°-15° C. To the resulting slurry was added 4-chlorophenylacetic acid (34.12 g). The resulting mixture was stirred at room temperature for one half hour and then heated to 70°-80° C. during 5.5 hours, during which time the mixture became effervescent. The reaction mixture was cooled and poured slowly onto cracked ice. The resulting suspension was brought to pH 10 with solid potassium carbonate. Ice was added intermittently during this addition to maintain the temperature below 15° C. Toluene (150 ml) was added and the resulting mixture heated at 100° C. for one hour. The mixture was cooled and allowed to stand overnight. The two resulting layers were separated and the aqueous layer extracted with toluene (2×100 ml). The combined organic layers were washed with water (5×200 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated in vacuo and the resulting yellow solid was triturated with hexane to yield 26 g of 2-(4-chlorophenyl)-3-dimethylaminopropenal as a tan solid mp. 120°-125° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728715
Quelldatensatzuspto-grants-1998_03
ORD IDord-351246f0dd44448ebbd806606156bbea
Quellennotizuspto-grants-1998_03