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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260886Generated: November 2, 2026

Chlorotrimethylsilane → HCID 15126108, compound

https://huagongshe.com/reaction/2260886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantHexamethyldisilazaneHCID 13838—
ReactantSodium BicarbonateHCID 516892—
Reactant1-O-Acetyl-5-O-t-butyldiphenylsilyl-4-thio-2,3-dideoxyribofuranoseHCID 15126098—
ReactantPotassium perfluorobutanesulfonateHCID 23675274—
ReactantCytosineHCID 178418229—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 15126108HCID 15126108—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 10 (0.26 g, 0.63 mmol), cytosine (0.105 g, 0.95 mmol), and potassium nonafluorobutanesulfonate (0.77 g, 2.3 mmol) was suspended in 12 mL dry acetonitrile under nitrogen. HMDS (0.135 mL, 0.63 mmol) and TMS-Cl (0.37 mL, 2.9 mmol) were added sequentially via syringe and the reaction stirred at 25° C. overnight. The reaction was poured into a mixture of 20 mL dichloromethane and 15 mL saturated NaHCO3 and shaken. The organic phase was dried (MgSO4) and concentrated in vacuo. The anomeric mixture was separated by preparative TLC with 7.5% MeOH/CHCl3 with an ammonia atmosphere: yield of β-anomer, 78 mg and 117 mg of the α-anomer to afford total yield of 195 mg (66.5% ); FAB MS 466 (M+H)+ ; 1H NMR (CDCl3) of α/β anomer, δ 8.12 (d, 1, 6-H) , 7.7 (m, 4, ArH), 7.4 (m, 6, ArH), 6.32 (m, 1, i'-H), 5.9-5.3 (hump, 1, NH2), 5.75 (d, 1, 5-H), 5.45 (d, 1, 5-H), 3. 75 (m, 3, 4'-Hα,β 's, 3'-Hα,β 's).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478928
Source datasetuspto-grants-1995_12
ORD IDord-7c18e03347c0461da7b4fa1e0501425b
Source noteuspto-grants-1995_12