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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1648974Erstellt: 25. Oktober 2026

4-Methoxyphenol → Butyl-a-bromoacrylate

https://huagongshe.com/reaction/1648974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethoxyphenolHCID 9015—
EduktPotassium HydroxideHCID 14797—
EduktPropanoic acid, 2,3-dibromo-, butyl esterHCID 519844—
ProduktButyl-a-bromoacrylateHCID 1990194872%

Reaktionsschritte

n-Butyl 2,3-dibromopropionate (144 g, 0.5 mole) containing p-methoxyphenol (0.5 g) was stirred vigorously under nitrogen and at room temperature, whilst 20% w/v aqueous caustic potash solution was slowly added. The course of the dehydrobromination was constantly monitored by gas-liquid chromatography. From time to time the reaction mixture was allowed to separate and the almost neutral aqueous phase discarded, in order to maintain that effective concentration of the added base. When more than 95% of the starting material had been consumed, the reaction was stopped and the lower organic layer run off and washed with water. After drying (Na2SO4), the crude product was distilled to give a main fraction which was n-butyl 2-bromoacrylate (yield 72%), bp 92°/17 mmHg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04414391
Quelldatensatzuspto-grants-1983_11
ORD IDord-38dbd090df094405a002ab58ce1d4c78
Quellennotizuspto-grants-1983_11