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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298788Generated: October 25, 2026

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

https://huagongshe.com/reaction/2298788

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 (Compound 21) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495532B1
Source datasetuspto-grants-2002_12
ORD IDord-8c2085c45b45400c882c1a8b0cd63444
Source noteuspto-grants-2002_12