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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376414Generated: October 30, 2026

2,3-Dihydrofuran → 1,3-O-di-(t-butyldimethylsilyl)-2-O-tetrahydrofuranylglycerol

https://huagongshe.com/reaction/376414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DihydrofuranHCID 70934—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant4,8-Dioxa-3,9-disilaundecan-6-ol, 2,2,3,3,9,9,10,10-octamethyl-HCID 10758091—
Solvent1,4-DioxaneHCID 31275—
Product1,3-O-di-(t-butyldimethylsilyl)-2-O-tetrahydrofuranylglycerolHCID 19361264100%

Reaction Steps

In dioxane was dissolved 3.45 g (11 mmol) of 1,3-O-di-(t-butyldimethylsilyl)glycerol followed by addition of 3.03 g (12 mmol) of pyridinium p-toluenesulfonate. To this suspension was added 16.5 ml (22 mmol) of dihydrofuran gradually under ice-cooling and the mixture was stirred for 1 hour. After return to ambient temperature, the mixture was allowed to react overnight. After completion of the reaction, the solvent was distilled off and the residue was treated with methylene chloride and saturated aqueous sodium hydrogen carbonate solution. The methylene chloride layer was washed with water, dried, and concentrated to provide 4.25 g (100%) of 1,3-O-di-(t-butyldimethylsilyl)-2-O-tetrahydrofuranylglycerol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020317
Source datasetuspto-grants-2000_02
ORD IDord-452df22ba2ee4de9a642527daadbff43
Source noteuspto-grants-2000_02