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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724761Generated: October 26, 2026

Oleyl p-toluenesulfonate → 1,3-O-dioleyl-2-O-tetrahydrofuranylglycerol

https://huagongshe.com/reaction/724761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOleyl p-toluenesulfonateHCID 11258749—
Reactant2-O-tetrahydrofuranylglycerolHCID 19361256—
ReactantHCID 178418922HCID 178418922—
SolventO-XyleneHCID 7237—
Product1,3-O-dioleyl-2-O-tetrahydrofuranylglycerolHCID 7025637418%

Reaction Steps

In 30 ml of xylene was dissolved 854 mg (5.3 mmol) of 2-O-tetrahydrofuranylglycerol. To this was added 1.78 g (15.9 mmol) of t-butoxypotassium under argon gas and the mixture was stirred for 5 minutes. Then, 10 ml of a solution of 6.71 g (15.9 mmol) oleyl p-toluenesulfonate in xylene was added dropwise and the mixture was stirred under reduced pressure (20-30 mmHg) at ambient temperature for 30 minutes and further at 50° C. for 1 hour. This reaction mixture was poured in ice-water and extracted with ether, and the extract was washed with water, dried, and concentrated. The residue was purified by column chromatography (silica gel/chloroform) to provide 628 mg (18%) of 1,3-O-dioleyl-2-O-tetrahydrofuranylglycerol as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705188
Source datasetuspto-grants-1998_01
ORD IDord-9357d88419b74d578cfe1241262cd1df
Source noteuspto-grants-1998_01