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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663553Generated: October 26, 2026

Trimethylsilyl triflate → Phenyl 2-o-acetyl-3,5-di-o-benzyl-4-c-methanesulfonyloxymethyl-1-thio-beta-d-ribofuranoside

https://huagongshe.com/reaction/1663553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl triflateHCID 65367—
ReactantPhenylthiotrimethylsilaneHCID 78312—
ReactantMethyl 2-O-acetyl-3,5-di-O-benzyl-4-C-methanesulfonyloxymethyl-D-ribofuranosideHCID 11145450—
SolventDichloromethaneHCID 6344—
ProductPhenyl 2-o-acetyl-3,5-di-o-benzyl-4-c-methanesulfonyloxymethyl-1-thio-beta-d-ribofuranosideHCID 1094081766.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Method a. A stirred solution of 209 (738 mg, 1.49 mmol) in anhydrous dichloromethane (6.4 mL) was added phenylthiotrimethylsilane (2.42 mL, 12.8 mmol) and cooled to 0° C. Trimethylsilyl triflate (0.67 mL, 3.67 mmol) was added dropwise and the solution was stirred at room temperature for 4 h. The reaction was quenched with a saturated aqueous solution of sodium hydrogen carbonate (100 mL) and extracted with dichloromethane (2×200 mL). The combined extract was dried (MgSO4) and the solvent removed by distillation under reduced pressure. The residue was purified by chromatography over silica gel with dichloromethane as eluent to give the product 210 as a clear oil (564 mg, 66%) and unreacted starting material (191 mg, 26%); Method b. A stirred solution of 211 (86 mg, 0.165 mmol) in anhydrous dichloromethane (0.49 mL) was added phenylthiotrimethylsilane (0.16 mL, 0.825 mmol) and cooled to 0° C. Trimethylsilyl triflate (0.037 mL, 0.206 mmol) was added and the solution was stirred at room temperature for 2 h. The reaction was quenched with a saturated aqueous solution of sodium hydrogen carbonate (15 mL) and the resulting mixture was extracted with dichloromethane (2×25 mL). The combined extract was dried (MgSO4) and the solvent removed by distillation under reduced pressure. The residue was purified by chromatography over silica gel with dichloromethane as eluent to give the product 210 as a clear oil (75 mg, 79%); 1H NMR (CDCl3): δ 7.47-7.19 (15 H, m, Bn, SPh), 5.48 (1 H, d, J 3.6 Hz, H-2), 5.34 (1 H, dd, J 3.7, 5.2 Hz, H-1), 4.54-4.36 (7 H, m, H-3, H-5□, Bn), 3.66 (1 H, d, J 9.7 Hz, H-5), 3.48 (1 H, d, J 9.5 Hz, H-5), 2.89 (3 H, s, SO2CH3), 2.09 (3 H, s, OCCH3); 13C NMR (CDCl3): δ 169.93 (C═O), 137.69, 137.08, 132.65, 132.45, 129.15, 128.53, 128.52, 128.18, 128.14, 128.08, 127.91, 127.85 (Bn, SPh), 87.99, 84.35, 80.34, 75.33, 74.20, 73.67, 70.83, 69.34 (C-1, C-2, C-3, C-4, C-5, C-5′, Bn), 37.27 (SO2CH3), 20.68 (OCCH3); MS FAB: 463 (M−SPh, 100%), 595 (M+Na, 24%); Found: C, 61.17; H, 5.55; C29H32O8S2 requires C, 60.82; H, 5.63%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034909B2
Source datasetuspto-grants-2011_10
ORD IDord-5dc8b19b10784e5290b3d6ad670a6492
Source noteuspto-grants-2011_10