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HRID 50583Erstellt: 24. Oktober 2026

Diethylene Glycol Monomethyl Ether → Ethyl 2,5,8,11,14,17,20,23-octaoxanonacosan-29-oate

https://huagongshe.com/de/reaction/50583

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethylene Glycol Monomethyl EtherHCID 8134—
EduktSodium hydrideHCID 24758—
Edukt6-{2-[2-(2-{2-[2-(2-Methylsulfonylethoxy) ethoxy]ethoxy}-ethoxy)-ethoxy]-ethoxy}-hexanoic acid ethyl esterHCID 86587027—
LösungsmittelTolueneHCID 1140—
ProduktEthyl 2,5,8,11,14,17,20,23-octaoxanonacosan-29-oateHCID 7136671762,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

NaH (88 mg of a 60% dispersion in oil, 2.2 mmol) was suspended in anhydrous toluene (3 ml) under N2 and chilled to 0° C. Non-polydispersed diethylene glycol monomethyl ether (0.26 ml, 0.26 g, 2.2 mmol) that had been dried via azeotropic distillation with toluene was added. The reaction mixture was allowed to warm to room temperature and stirred for four hours, during which time the cloudy grey suspension became clear and yellow and then turned brown. Mesylate 20 (0.50 g, 1.0 mmol) in 2.5 ml dry toluene was added. After stirring at room temperature over night, the reaction was quenched by the addition of 2 ml of methanol and the resultant solution was filtered through silica gel. The filtrate was concentrated in vacuo and the FAB MS: m/e 499 (M+H), 521 (M+Na). Additional purification by preparatory chromatography (silica gel, 19/3 chloroform/methanol) provided the non-polydispersed product as a clear yellow oil (0.302 g 57%). FAB MS: m/e 527 (M+H), 549 (M+Na).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713452B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-dd254f3cb7854e2ea9bea3f6e077f602
Quellennotizuspto-grants-2004_03