HCID 11167178, compound → HCID 54028878, compound

HRID 466901Notes

Reaction equation

HRID 466901 reaction equation
[CH2:1]([O:8][C@@H:9]1[C@@H:16]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C@@H:15]([OH:25])[C@@H:14]([CH2:26][O:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[O:13][C@@H:10]1[O:11]C)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>FC(F)(F)C(O)=O.O>[CH2:1]([O:8][C@@H:9]1[C@@H:16]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C@@H:15]([OH:25])[C@@H:14]([CH2:26][O:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[O:13][CH:10]1[OH:11])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Conditions

Temperature
0 °C

Procedure

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.

Workup

  1. customThe solvents are evaporated under reduced pressure
  2. temperaturewithout heating
  3. dissolutionThe residue is dissolved in ethyl acetate
  4. washwashed successively with sodium bi-carbonate and brine
  5. dry with materialThe organic layer is dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure so as
  8. customto afford an oil
  9. washFlash chromatography on silica gel and elution
  10. additionwith a graded mixture of ethyl acetate and hexane

Sources & evidence

ORD record
ord-85d78a1daf484df781830bf755f5cd30
Source dataset
uspto-grants-1992_10
Patent number
US05157116

Reaction notes

Loading…