HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Bromide ion
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2,3,4,5,6-Penta-O-acetyl-D-glucose | HCID 92972 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Bromide ion | HCID 259 | — |
| Product | 2,3,4,5,6-Penta-O-acetyl-D-glucose | HCID 92972 | — |
Reaction Steps
To a 500 ml flask was added 50 g of glucose pentaacetate (C6H22O11) and 80 ml of methylene chloride. The mixture was stirred at ice-water bath for 20 min HBr in HOAc (33%, 50 ml) was added to the reaction mixture. After stirring for 2.5 hr another 5 ml of HBr was added to the mixture. After another 30 min, the mixture was added 600 ml of methylene chloride. The organic mixture was washed with cold water (200 ml×2), Saturated NaHCO3(200 ml×2), water (200 ml) and brine (200 ml×2). The organic layer was dried over Na2SO4 and the mixture was evaporated at RT to give white solid as final product, bromide derivative, IntD1 (˜95% yield). C14H19BrO9, TLC Rf=0.49, SiO2, 40% ethyl acetate/60% hexanes; Exact Mass 410.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288515B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-ee1ced95edc2487ab092b72917741c95 |
| Source note | uspto-grants-2012_10 |