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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279905Erstellt: 25. Oktober 2026

Allyl bromide → alpha-Allylbenzoin methyl ether

https://huagongshe.com/reaction/279905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktMethyl BenzoinHCID 98097—
EduktPotassium tert-butoxideHCID 23665647—
Lösungsmitteltert-ButanolHCID 6386—
Produktalpha-Allylbenzoin methyl etherHCID 2044199083,6%

Reaktionsschritte

Benzoin methyl ether (50 g) and t-butanol (500 g) were added to a 1 liter, 3-neck round bottom flask equipped with magnetic stirrer, and placed in an oil bath at 80° C. To this mixture, 33.7 g of potassium t-butoxide was added and the solution stirred for 15 minutes. Allyl bromide (42.3 g) was added dropwise over a 1 hour period and stirring was continued at 85° C. for 2 more hours followed by cooling to room temperature. After evaporation of t-butanol and filtration of potassium bromide, the product was distilled at 125° C.±2° C. and 0.05 mm Hg to yield 49.2 g of α-allylbenzoin methyl ether which crystallized upon cooling.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04587276
Quelldatensatzuspto-grants-1986_05
ORD IDord-4b74e43a74af4b369025d24061fc87ed
Quellennotizuspto-grants-1986_05