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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 444062Erstellt: 24. Oktober 2026

Allyl bromide → 1,2-di-O-(n-hexadecyl)-3-allyl-glycerol

https://huagongshe.com/de/reaction/444062

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktSodium hydrideHCID 24758—
Edukt2,3-Bis(hexadecyloxy)propan-1-olHCID 102548—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt1,2-di-O-(n-hexadecyl)-3-allyl-glycerolHCID 2346610393%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

Sodium hydride (1.78 g. of 50 wt. % dispersion in mineral oil, 37 mmoles) was added at 60° C. to a solution of 1,2-di-O-(n-hexadecyl)-glycerol (10 g., 18.5 mmoles) in N,N-dimethylformamide (100 ml.), and the resulting solution stirred for 20 minutes at 60° C. Allyl bromide (4.47 g., 37 mmoles) was then added dropwise and the resulting mixture stirred for 3 hours at 90° C., cooled, cautiosly diluted with water (200 ml.) to quench the reaction, and extracted with ether (3×150 ml.). The combined ether extract was washed with saturated aqueous sodium chloride solution, dried (MgSO4), filtered and evaporated in vacuo to an oil, which was purified by silica gel chromatography (elution with benzene) [10 g., 93% yield, oil, n.m.r. (CDCl3) δ 5.66-6.16 (m, 1, --OCH2CH=CH2), 5.25 (d of doublets, 2, --OCH2CH=CH2) and 4.03 (d, 2, --OCH2CH=CH2)].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04262021
Quelldatensatzuspto-grants-1981_04
ORD IDord-3d85f4df80d5446fb0f8780c35a4b914
Quellennotizuspto-grants-1981_04