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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417176Generated: November 2, 2026

Triethylamine → allyl-3-O-methyl-glucopyranose

https://huagongshe.com/reaction/1417176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantD-Glucoyranose, 3-O-methyl-HCID 96241—
SolventTrifluoroacetic acidHCID 6422—
SolventAllyl AlcoholHCID 7858—
Productallyl-3-O-methyl-glucopyranoseHCID 13172002150.8%

Reaction Steps

3-O-methyl-1,2:5,6-di-O-isopropylidine-glucopyranose (10.2 g) was dissolved in 90% aqueous trifluoroacetic acid (30 mL) and stirred for 1 hour at room temperature. The reaction mixture was evaporated and then coevaporated with toluene followed by ethanol coevaporation to provide the product which was directly used for further allyl glycosylation. 7.9 g of 3-O-methyl-glucopyranose was dissolved in 50 mL of dry allyl alcohol and 120 μL of trifluoromethanesulfonic acid was added. The mixture was heated for 51/2 h at 80° C. Triethylamine (1 mL) was added to destroy excess trifluoromethanesulfonic acid, evaporated and coevaporated with water to remove allyl alcohol. The material was purified by chromatography on silica gel using dichloromethane-methanol (20:1) as eluent to yield allyl-3-O-methyl-glucopyranose (4.85 g, 50.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877157
Source datasetuspto-grants-1999_03
ORD IDord-c5e69cb979e84d398c3fb6493b780f1d
Source noteuspto-grants-1999_03