Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | D-Galactal | HCID 2734735 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | D-(+)-Glucal | HCID 2734736 | — |
Reaction Steps
Galactal 7′ (0.100 g, 0.304 mmol) in 5 mL dry CH2Cl2 at 0° C. under a N2 atmosphere was treated with 10 mL Murray solution (freshly prepared) and stirred at 0° C. for 40 min. TLC (1:1 EtOAc:hex) showed no trace of 7′. Solvents were evaporated using a dry N2 stream. The residual epoxide of 7′ was kept on a vac. line ˜2 h. To the epoxide under a N2 atmosphere was added a solution of glucal derivative 3′ (0.150 g, 0.496 mmol) in 3 mL dry THF. On cooling to −78° C., 1.0 M ZnCl2 in Et2O (0.50 mL, 0.50 mmol) was added. The mixture was allowed to slowly warm to r.t. (over ˜2 h) and stirred overnight. TLC (1:1 EtOAc:hex) showed that the reaction was complete. Saturated aq. NaHCO3 (20 mL) was added, and the mixture was then extracted with EtOAc (3×20 mL). The organic layer was dried over MgSO4. Column chromatography on silica (1:3 EtOAc:hex) afforded diol 18′ as a colorless solid. Yield: 173 mg (89%). [α]D23−9.8° (c 1.0, CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06645935B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-47b719b9651f498bab27e5dcab151d2a |
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| Source note | uspto-grants-2003_11 |
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