Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 69732337 | HCID 69732337 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 69732883 | HCID 69732883 | 89% |
Reaction Steps
[Litt=S. Andersen et al. J. Carbohydrate Chemistry, 17 (1998) 1027-1035, P. Jarglis and F. W. Lichtenthaler. Angew. Chem. 94 (1982) 140-141 with a benzoylated analog]. To a solution of 3,4,6-tri-O-acetyl-1,5-anhydro-D-fructose (3) (2.21 g, 7.67 mmol) in dry acetone (77 mL), anhydrous NaOAc (2.2 g) was added and the reaction mixture was stirred for 3 h. The salts were filtered off and washed with acetone. The filtrate was concentrated and purified by column chromatography (30 g silica, eluted with hexane-EtOAc. 2:1) to give 4 as a syrup (1.56 g, 89%): 1H NMR (CDCl3 at 7.27, 300 MHz) δ 2.12 (s, 3H, OCOCH3), 2.26 (s, 3H, OCOCH3), 4.24 (dd, J=4.0 and 12.0, 1H, H-6), 4.25 (dd, J=2.0 and 16.5, 1H. H-1), 4.42 (dd, J=6.0 and 12.0, 1H, H-6′), 4.46 (d, J=16.5, 1H, H-1′), 4.80 (dddd, J=2.0, 2.0, 4.0 and 6.0, 1H, H-5), 6.59 (d, J=2.0, 1H, H-4). 13C NMR (CDCl3 at 77.0, 50.3 MHz) δ 20.3-20.7 (2×OCOCH3), 64.4 (C-6), 71.4 (C-1), 72.6 (C-5), 132.8 (C-4), 143.8 (C-3), 168.1-170.7 (2×OCOCH3), 187.7 (C-2)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06846505B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-4ec1697872f14f0cb6438544555239b3 |
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| Source note | uspto-grants-2005_01 |
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