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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977280Generated: October 30, 2026

Methyl iodide → (+/-)-1-S-hexadecyl-2-O-methyl-3-O-tritylthioglycerol

https://huagongshe.com/reaction/977280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-Hexadecylthio-3-trityloxy-2-propanolHCID 13002864—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-1-S-hexadecyl-2-O-methyl-3-O-tritylthioglycerolHCID 14522774101.9%

Reaction Steps

A solution of 6.0 grams (0.01 mole) (±)-1-S-hexadecyl-3-O-tritylthioglycerol in 250 milliliters of THF was added to a slurry of 0.4 grams (0.014 mole) 80% NaH (oil dispersion) in 50 milliliters of THF and the reaction mixture stirred at room temperature for one hour. Then 1.4 gram (0.13 mole) of CH3I was added and the reaction allowed to proceed at room temperature for 24 hours. The reaction mixture was then diluted with 300 milliliters of distilled water and extracted twice with 200 milliliter portions of ether. The nonaqueous extracts were combined, dried over anhydrous sodium sulfate, filtered and removed in vacuo to provide 6.0 grams of crude product as an oil. 1H-NMR (CDCl3): delta, 0.7-1.7[m, 31H, (CH2)14CH3 ], 2.3-2.8(m, 4H, CH2 --S--CH2), 3.25(m, 5H, CH3O, CH--CH2 --O), 3.6-4.0(m, 1H, CH), 7.6-7.0[m, 15H, C(C6H5)3 ].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614548
Source datasetuspto-grants-1997_03
ORD IDord-7fc21e71970948598b1eadaee890ab83
Source noteuspto-grants-1997_03