HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 1,3,5-tri-O-benzoyl-alpha-L-ribofuranose
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ribofuranose, 1-acetate 2,3,5-tribenzoate | HCID 10973190 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,3,5-tri-O-benzoyl-alpha-L-ribofuranose | HCID 11048843 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Compound 10 (9 g, 17.84 mmol) was stirred in 100 ml of CH2Cl2 at 0° C. while 70 ml of CH2Cl2 containing HBr (3.2 g, 30.5 mmol) was added in one portion. The mixture was stirred at 0° C. for 3.5 hrs, water (55 ml) was added and the mixture stirred at r.t. for 18 hrs. The organic layer was separated, washed with sat. NaHCO3, dried (MgSO4). After evaporation of the solvent, a foam was obtained, which upon recrystallization from CH2Cl2 and n-hexane, gave 11 as a white solid. (6.2 g, 75.5%). m.p. 137°-138° C., lit. 140°-141° C., [α]D =-81.960 (c 0.55, CHCl3 ; D form: [α]D =+83.71.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05567688 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-573ee56e06e947699ef64d94373d05f7 |
| Source note | uspto-grants-1996_10 |