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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466901Generated: October 29, 2026

HCID 11167178, compound → HCID 54028878, compound

https://huagongshe.com/reaction/466901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11167178HCID 11167178—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 54028878HCID 54028878—

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl 2,3,6-tri-O-benzyl-α-D-galactopyranoside (5 g, 10.75 mmol) is dissolved at 0° C. in a 9:1 mixture of trifluoroacetic acid and water (50 mL) (N. Morishima, S. Koto, M. Oshima, A. Sugimoto and S. Zen, Bull Chem. Soc. Jpn 56, 2849 (1983)). The mixture is stirred overnight at 0° C. The solvents are evaporated under reduced pressure without heating. The residue is dissolved in ethyl acetate and washed successively with sodium bi-carbonate and brine. The organic layer is dried over sodium sulfate, filtered and concentrated under reduced pressure so as to afford an oil. Flash chromatography on silica gel and elution with a graded mixture of ethyl acetate and hexane will afford 2,3,6-tri-O-benzyl-D-galactopyranose as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157116
Source datasetuspto-grants-1992_10
ORD IDord-85d78a1daf484df781830bf755f5cd30
Source noteuspto-grants-1992_10