HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Heptaacetate bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | D-Glucose | HCID 5793 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Heptaacetate bromide | HCID 86737203 | — |
Reaction Steps
Glc 1β,4 glc is converted to its octaacetate form by conventional methods as disclosed in Methods in Carbohydrate Chemistry 1, 334. A 20 g. portion of this octaacetate is dissolved in 200 ml. of methylene chloride and the solution is cooled to 0° C. An 80 ml. portion of 32% hydrobromic acid in glacial acetic acid is added and the mixture is allowed to stand in an ice bath for 2 hours. The mixture is then poured into crushed ice and diluted with 200 ml. of methylene chloride. The organic layer is separated, washed repeatedly with ice water until neutral, dried over anhydrous sodium sulfate and evaporated in vacuo, giving glc 1β,4 glc heptaacetate bromide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232150 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-68f0f92c196f49ada6b8e9f4caf4dc85 |
| Source note | uspto-grants-1980_11 |