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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 555974Erstellt: 25. Oktober 2026

3-Phenylprop-2-Enal → alpha-Bromocinnamaldehyde

https://huagongshe.com/reaction/555974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Phenylprop-2-EnalHCID 307—
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
EduktBromineHCID 24408—
LösungsmittelAcetic AcidHCID 176—
Produktalpha-BromocinnamaldehydeHCID 21585—

Reaktionsschritte

1.33 g (10 mmol) cinnamaldehyde was dissolved in 5 mL glacial acetic acid and cooled on an ice-water bath. 1.62 g bromine was added, and anhydrous K2CO3 was then added, and it was stirred until no gas was evolving. After refluxing for 30 min, the reaction mixture was poured into 100 mL cold water with stirring, extracted with 50 mL ethyl ether three times. The combined ethyl ether layers were washed with water one time, saturated aqueous NaCl solution one time, dried over MgSO4 for 2 hours, filtrated, and the filtrate was dried under vacuum, and washed with anhydrous ethyl ether: petroleum ether (1:1) to give the title compound as light yellow powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08053577B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-33127781f18340369da56dfe4b8793c5
Quellennotizuspto-grants-2011_11