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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227218Generated: October 31, 2026

Trimethylsilyl triflate → HCID 53700596, compound

https://huagongshe.com/reaction/2227218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl triflateHCID 65367—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
ReactantTri-O-acetyl-5-deoxy-D-ribofuranoseHCID 11196237—
ReactantHCID 18472159HCID 18472159—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 53700596HCID 5370059655.9%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413938B1
Source datasetuspto-grants-2002_07
ORD IDord-62129636baaf43248e9cfa8bf5b031cc
Source noteuspto-grants-2002_07