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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 500288Erstellt: 24. Oktober 2026

Ethylene Glycol → 2-((3-Methyloxetan-3-yl)methoxy)ethanol

https://huagongshe.com/de/reaction/500288

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktPotassium HydroxideHCID 14797—
EduktOxetane, 3-(bromomethyl)-3-methyl-HCID 144860—
Produkt2-((3-Methyloxetan-3-yl)methoxy)ethanolHCID 6867658429,3%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Ethylene glycol (26.25 g, 0.42 mol) and KOH (19.45 g, 0.35 mol) were added to a round-bottom flask equipped with a magnetic stirrer and a reflux condenser. When all KOH had dissolved the 3-bromomethyl-3-methyloxetane (4) (46.30 g, 0.28 mol) was added. The system was heated to 70° C. for 3 hours. The reaction material was then distilled under vacuum (10 Torr) and collected as a single fraction. The distilled material was then extracted with diethyl ether and water. The water fraction was then extracted with CHCl3 multiple times to obtain 11.98 g (29.2% yield) of the final product, though analysis of the water phase indicated a significant amount of HE1Ox was unextracted. H1 NMR (CDCl3): δ 1.31 ppm (—CH3, 3H, s), δ 2.63 ppm (—OH, 1H, t), δ 3.54 ppm (—CH2—, 2H, s), δ 3.60 ppm (—OCH2—, 2H, t), δ 3.76 ppm (HOCH2—, 2H, q), δ 4.38 ppm (oxetane CH2, 2H, d), δ 4.55 ppm (oxetane CH2, 2H, d).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07771793B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-6af57866122e4615bd7f87372ffbc2db
Quellennotizuspto-grants-2010_08