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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501903Generated: November 2, 2026

Acetonitrile → HCID 67327008, compound

https://huagongshe.com/reaction/1501903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTrityl chlorideHCID 6456—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 86657041HCID 86657041—
SolventTriethylamineHCID 8471—
ProductHCID 67327008HCID 6732700879%

Reaction Steps

20 grams of 1-eicosanyl-sn-glycerol and 18 grams of triphenylchloromethane were added to a mixture of 400 ml dry tetrahydrofuran (THF) and 100 ml dry acetonitrile. 15 ml of dry triethylamine was added, and the reaction mixture was refluxed for 17 hours. The reaction mixture was then cooled to room temperature, poured on ice (500 grams), transferred to a separatory funnel, and extracted thrice with 200 ml diethyl ether. The organic phase was washed consecutively with 150 ml water, twice with 150 ml dilute (1.5%) H2SO4, 150 ml water, 150 ml concentrated aqueous sodium bicarbonate, and again with 150 ml water. The solution was then dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. The obtained residue, a brown oil, was dissolved in 300 ml ethyl acetate, and cooled at −20° C. overnight. The mixture was centrifuged (3,500 rotations per minute) at −10° C., and the mother liquid was poured of. The obtained solid was dissolved in hexane and refrigerated (5±3° C.) overnight. Filtration of the precipitate yielded 26.0 grams of pure (R)-1-eicosanyl-3-trityl-sn-glycerol as an off-white solid. The yield was 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206206B2
Source datasetuspto-grants-2015_12
ORD IDord-9103c8f95b7f476e89dc772693ef7779
Source noteuspto-grants-2015_12