HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227218Generated: October 31, 2026
Trimethylsilyl triflate → HCID 53700596, compound
https://huagongshe.com/reaction/2227218
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Reactant | Tri-O-acetyl-5-deoxy-D-ribofuranose | HCID 11196237 | — |
| Reactant | HCID 18472159 | HCID 18472159 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 53700596 | HCID 53700596 | 55.9% |
Reaction Steps
To a suspension of 4-bromo-2,5,6-trichloro-1H-benzimidazole (0.30 g, 1 mmol), in acetonitrile (5 mL) was added N,O-bis(trimethylsilyl)acetamide (0.25 mL, 1 mmol). The resulting mixture was allowed to stir at 65° C. for 15 min., followed by the addition of 1,2,3-tri-O-acetyl-5-deoxyribofuranose (0.31 g, 1.2 mmol) in acetonitrile (5 mL) and trimethylsilyltrifluoromethane sulfonate (0.25 mL, 1.3 mmol). The mixture was allowed to stir at 65° C. for 20 min and was then allowed to cool to RT. The mixture was diluted with ethyl acetate and was washed with a saturated NaHCO3/NaCl solution, dried over MgSO4 and the solvents were removed by rotary evaporation. The product was purified by flash chromatography using chloroform as eluent followed by recrystallization from methanol to provide 0.28 g (55%) of the title compound as white crystals; m.p. 138-141° C.; 1H NMR (DMSO-d6) δ: 8.18 (s, 1H), 6.19 (d, 1H), 5.61 (dd, 1H), 5.25 (dd, 1H), 4.24 (m, 1H), 2.14 (s, 3H), 2.02 (s, 3H), 1.50 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413938B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-62129636baaf43248e9cfa8bf5b031cc |
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| Source note | uspto-grants-2002_07 |
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