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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | methyl 2,3,5-tri-O-benzyl-L-xylofuranoside | HCID 11015596 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2,3,5-tri-O-benzyl-L-xylofuranose | HCID 131717204 | 53% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05097023 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-0eb5f4b01683457591f7aefafea005cd |
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| Source note | uspto-grants-1992_03 |
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