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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 970764Erstellt: 24. Oktober 2026

Phosphorus oxychloride → 3-Methyl-5-phenyl-2,4-pentadienoic acid

https://huagongshe.com/de/reaction/970764

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphorus oxychlorideHCID 24813—
Edukt3-Methyl-1-phenyl-buten-3-olHCID 92677—
EduktSodium AcetateHCID 517045—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Methyl-5-phenyl-2,4-pentadienoic acidHCID 77493863,4%

Reaktionsschritte

Dimethylformamide (DMF, anhydrous, 25 mL) was cooled to 0–5° C. and phosphorus oxychloride (16.4 mL) was added dropwise over a period of an hour. The resulting solution was added dropwise to a cooled (0–5° C.) solution of 4-phenyl-2-methyl-3-buten-2-ol (0.14 mol) in 60 mL of anhydrous DMF over a period of an hour. The reaction mixture was then warmed to room temperature, gradually heated up to 80° C., stirred at 80° C. for three hours and cooled to 0–5° C. To the cooled reaction solution was added dropwise a solution of sodium acetate (80 g) in deionized water (190 mL) over a period of two hours. The mixture was then reheated to 80° C., stirred at 80° C. for an additional 10 minutes, cooled down to room temperature and extracted with ether (300 mL) twice. The combined extract was washed with water (200 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum to yield 16.7 g of the desired 3-methyl-5-phenyl-2,4-pentadienal as a liquid which was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07312247B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-0a2272a7ab504bc09469b8a7fe8369d1
Quellennotizuspto-grants-2007_12