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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653981Generated: October 26, 2026

Chlorotrimethylsilane → HCID 15126108, compound

https://huagongshe.com/reaction/653981

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, 1'-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 numberUS05128458
Source datasetuspto-grants-1992_07
ORD IDord-e369a01e7e4949d5a42ef03f07094859
Source noteuspto-grants-1992_07