HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 67404620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | D-Galactopyranose, 3-deoxy-3-[(3,5-dimethoxybenzoyl)amino]-, 1,2,4,6-tetraacetate | HCID 67405050 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67404620 | HCID 67404620 | — |
Reaction Steps
1,2,4,6-Tetra-O-acetyl-3-deoxy-3-(3,5-dimethoxybenzamido)-D-galactopyranose 4 (50 mg, 0.098 mmol) was dissolved in dichloromethane (1 ml) which had been dried over 4 Å molecular sieves. Acetic anhydride (18 μl, 0.20 mmol) and HBr (0.2 ml, 33% in AcOH) were added, and the mixture was stirred under N2 at room temperature. After 2 h 30 min, the reaction mixture was diluted with dichloromethane (30 ml) and poured into ice-water (30 ml). The organic phase was washed with NaHCO3 (30 ml of a saturated aqueous solution), dried (MgSO4), filtered and concentrated in vacuo to give 2,4,6-tri-O-acetyl-3-deoxy-3-(3,5-dimethoxybenzamido)-α-D-galactopyranosyl bromide 9, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07638623B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-a6da6e937d67498088a2bfd3dd05f861 |
| Source note | uspto-grants-2009_12 |