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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496993Generated: October 25, 2026

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

https://huagongshe.com/reaction/496993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
ReactantSelachyl alcoholHCID 5282282—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
Product1-o-Oleyl-2-o-methyl-3-o-trityl glycerolHCID 69470780—

Reaction Steps

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 (Cornpound 21) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949529B2
Source datasetuspto-grants-2005_09
ORD IDord-9a7a7b355b1a46eda5505c7a3f3adb6b
Source noteuspto-grants-2005_09