HuagongsheHuagongshe Chemistry Print Report · For research reference only
beta-Maltose → 2,3,4,6-Tetra-O-benzoyl-alpha-D-glucopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-D-glucopyranose
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | beta-Maltose | HCID 6255 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2,3,4,6-Tetra-O-benzoyl-alpha-D-glucopyranosyl-(1->4)-1,2,3,6-tetra-O-benzoyl-D-glucopyranose | HCID 86658290 | 163.2% |
Reaction Steps
Maltose (2.0 g, 5.84 mmol) was dissolved in dry pyridine (40 mL) at 0° C. DMAP (cat.) was added. Benzoyl chloride (2.5 equiv., 14.6 mmol, 16.4 g, 13.6 mL) was added dropwise and the solution stirred at room temperature overnight. The solution was poured onto a mixture of ice-water and DCM. The organic layer was washed with NaHCO3(sat.) (×7), brine, H2SO4 (5%) (×2), followed by brine. The solution was dried (Na2SO4) and the solvent evaporated. The product was passed through a short silica plug to remove the remaining benzoyl chloride and the solvent was evaporated to yield 3.5 g (51%) of the white solid product which was reacted on without further purification or characterisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08828952B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-92d75a399458477297c2157fe3ba3cf2 |
| Source note | uspto-grants-2014_09 |