HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2,5,6-Trichloro-1-(beta-D-arabinofuranosyl)benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | 2,5,6-Trichloro-1-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)benzimidazole | HCID 53992940 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,5,6-Trichloro-1-(beta-D-arabinofuranosyl)benzimidazole | HCID 53698358 | — |
Reaction Steps
Compound 133 (1.25 g 2 mmole) was dissolved in dry CH2Cl2 (20 ml) and this solution was cooled in an acetone-dry ice bath. A 1M solution of BCl3 in CH2Cl2 (10 ml) was added and the mixture was stirred at -70° for 4.5 hr. At this point TLC showed no starting material. CH3OH (10 ml) was added and the solution was made neutral with NH4OH. The solution was evaporated in vacuo to dryness. H2O (20 ml) was added and the solution was extracted with EtOAc. The EtOAc layer was washed with H2O, dried (Na2SO4) and evaporated in vacuo to obtain a syrup. This syrup was subjected to flash column chromatography on silica gel (Kieselgel 60, 230-400 mesh) with CH2Cl--MeOH (20:1) as eluent solvent to give 134. Yield 0.551 g, 77.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646125 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-50b963f64b68477098af92a6185dd1af |
| Source note | uspto-grants-1997_07 |