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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720178Generated: October 30, 2026

HCID 11167178, compound → HCID 54028878, compound

https://huagongshe.com/reaction/1720178

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, 10.775 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 bicarbonate 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 numberUS05504078
Source datasetuspto-grants-1996_04
ORD IDord-6cc86874b4904220905d88c0ca7c4af1
Source noteuspto-grants-1996_04