HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2,3,4-Tri-O-acetyl-6-deoxy-6-phthalimido-alpha-D-galactopyranosyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1,2,3,4-tetra-O-acetyl-6-deoxy-phthalimido-D-galactopyranose | HCID 54233455 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3,4-Tri-O-acetyl-6-deoxy-6-phthalimido-alpha-D-galactopyranosyl bromide | HCID 54166555 | 91% |
Reaction Steps
A solution of 1,2,3,4-tetra-O-acetyl-6-deoxy-phthalimido-D-galactopyranose (4.2 g.) in dichloromethane (2 ml.) is treated with 30-32% hydrobromic acid in glacial acetic acid (10 ml.) for 1 hour. The reaction mixture is poured into ice-water, and the product is immediately extracted with dichloromethane. The organic layer is washed with cold aqueous sodium hydrogencarbonate and cold water, dried, and evaporated in vacuo to give the title compound as a syrup (4.0 g., 91%); n.m.r. (chloroform-d): ∂ 6.63 (d, J1,2 4.0 Hz, H-1), 7.58-7.90 (4 aromatic), 1.96, 2.07 and 2.13 (3 OAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310505 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-4a533c16343a422c9a9e31a6962be18d |
| Source note | uspto-grants-1982_01 |