Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372145Generated: October 30, 2026

Trifluoroacetic acid → Methyl 2,3,5-tri-O-benzyl-L-xylofuranose

https://huagongshe.com/reaction/2372145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantmethyl 2,3,5-tri-O-benzyl-L-xylofuranosideHCID 11015596—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2,3,5-tri-O-benzyl-L-xylofuranoseHCID 13171720453%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl 2,3,5-tri-O-benzyl-L-xylofuranoside (22.7 g, 56.30 mmol) is dissolved at 0° C. in a 9:1 mixture of trifluoroacetic acid and water (200 mL) and stirred at 0° C. overnight. The mixture is put to dryness under reduced pressure. The oily residue is dissolved in ethyl acetate and washed three times with a saturated solution of sodium bicarbonate. The organic layer is dried over sodium sulfate, filtered and put to dryness under reduced pressure to afford an oil. Flash chromatography on silica gel and elution with a 7:3 mixture of cyclohexane and ethyl acetate yield methyl 2,3,5-tri-O-benzyl-L-xylofuranose as an oil (11.7 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05097023
Source datasetuspto-grants-1992_03
ORD IDord-0eb5f4b01683457591f7aefafea005cd
Source noteuspto-grants-1992_03