Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186431Generated: October 31, 2026

Chlorotrimethylsilane → HCID 11146723, compound

https://huagongshe.com/reaction/2186431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 11307367HCID 11307367—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 11146723HCID 1114672383.2%

Reaction Steps

Dried 5′-O-t-butyldiphenylsilyl-2′-O-(hydroxyethyl)-adenosine (24 g, 43.7 mmol) was dissolved in anhydrous pyridine (500 mL) under inert atmosphere, and trimethylchlorosilane (27.7 mL, 218 mmol) was added at 0° C. The reaction was allowed to warm to ambient temperature, stirred for 1 hour, then cooled to 0° C. Benzoyl chloride (25.3 mL, 218 mmol) was added dropwise, then the reaction was allowed to warm to ambient temperature and stirred for 4 hours after which it was cooled to 0° C. and water (100 mL) was added. After stirring for 10 minutes aqueous 30% NH4OH (100 mL) was added, and the reaction was stirred at 0° C. for 1 hour. The solvent was evaporated in vacuo to give a residue which was dissolved in EtOAc (1 L), and the resulting solution was washed with water (200 mL) twice, then with brine (100 mL). The organic solution was dried with MgSO4, and the solvent was evaporated in vacuo to give a residue. The residue was purified by column chromatography using CH2Cl2—EtOAc—MeOH, 70:27:3, to give the title compound as a solid (23.77 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403779B1
Source datasetuspto-grants-2002_06
ORD IDord-bd80b982668e44f2a0ad5ce7a19c9f01
Source noteuspto-grants-2002_06