Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 23396148 | HCID 23396148 | — |
| Reactant | HCID 178435178 | HCID 178435178 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 91272540 | HCID 91272540 | 75% |
Reaction Steps
To a mixture of methyl 2-azido-4-O-benzyl-6-O-tert-butyldiphenylsilyl-2-deoxy-3-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside (32) (1.5 g, 2.2 mmol) and anhydrous AcOH (28.8 mL) in dry THF (169 mL) hydrogen fluoride-pyridine complex (20.3 mL) was added in a polypropylene container. The reaction mixture was kept at room temperature overnight, then diluted with EtOAc (1 L). The resulting solution was washed with saturated sodium hydrogen carbonate (4×1 L), saturated brine solution (1 L), dried over MgSO4 and evaporated to dryness. The residue was crystallized from MeOH. The mother liquor was evaporated, the residue was treated with hexane to get more solid. The solid products were combined affording methyl 2-azido-4-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside (33) (735 mg, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953850B1 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-7ec0fb8768d14427aefa7ae19e35afc0 |
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| Source note | uspto-grants-2005_10 |
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