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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242017Erstellt: 24. Oktober 2026

Allyl bromide → Methyl 2-(allyloxy)propanoate

https://huagongshe.com/de/reaction/242017

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktMethyl LactateHCID 11040—
EduktSodium hydrideHCID 24758—
EduktSodium BicarbonateHCID 516892—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 2-(allyloxy)propanoateHCID 13971956—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

(±)-Methyl-2-hydroxypropanoate (7.6 g, 74 mmol) was dissolved in tetrahydrofuran (100 mL), cooled to 0° C. and treated with sodium hydride (3.6 g, 60% dispersion, 89 mmol, 1.2 equiv) portionwise over 45 minutes. The mixture was warmed to ambient temperature, stirred for 30 minutes, and then cooled to 0° C. Allyl bromide (8.4 mL, 96 mmol, 1.3 equiv) was added, the mixture was warmed to ambient temperature and stirred for an additional 14 hours. Sodium bicarbonate (10 mL, aqueous saturated) was added slowly and the mixture was stirred for 30 minutes before being poured into water (500 mL). The aqueous layer was extracted with ethyl acetate (2×300 mL) and the combined organic extracts were washed once with brine, dried with sodium sulfate, filtered and concentrated in vacuo, providing the titled compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653079B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-d4ecf825aa5b4d4e89202ad8f730cded
Quellennotizuspto-grants-2014_02