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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2298788Erstellt: 26. Oktober 2026

Methyl iodide → 1-o-Oleyl-2-o-methyl-3-o-trityl glycerol

https://huagongshe.com/reaction/2298788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktTrityl chlorideHCID 6456—
EduktSodium hydrideHCID 24758—
EduktSelachyl alcoholHCID 5282282—
LösungsmittelWaterHCID 962—
LösungsmittelPyridineHCID 1049—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-o-Oleyl-2-o-methyl-3-o-trityl glycerolHCID 69470780—

Reaktionsschritte

Diol Compound 20 (2.0 g, 5.97 mmol) was added dropwise to a solution of trityl chloride (1.66 g, 6.0 mmol) in anhydrous pyridine (10 mL). The reaction was left to stir for 16 hours after which the solvent was removed by co-evaporation with toluene (2×5 mL). Then, part of the residue (1.0 g, 1.7 mmol) was added dropwise to a suspension of NaH (0.14 g, 3.4 mmol) in THF (50 mL), followed by the addition of MeI (0.22 mL, 3.4 mmol). After 16 hours, TLC analysis showed that the reaction had gone to completion and H2O (5 mL) was added followed by concentration of the reaction mixture. The residue was partitioned between H2O (20 mL) and diethyl ether (100 mL), the organic extract was washed with sat. NaHCO3 (10 mL), dried (MgSO4) and concentrated to give 1-O-oleyl-2-O-methyl-3-O-trityl glycerol (Compound 21) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06495532B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-8c2085c45b45400c882c1a8b0cd63444
Quellennotizuspto-grants-2002_12