HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720178Generated: October 30, 2026
HCID 11167178, compound → HCID 54028878, compound
https://huagongshe.com/reaction/1720178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11167178 | HCID 11167178 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 54028878 | HCID 54028878 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05504078 |
|---|
| Source dataset | uspto-grants-1996_04 |
|---|
| ORD ID | ord-6cc86874b4904220905d88c0ca7c4af1 |
|---|
| Source note | uspto-grants-1996_04 |
|---|