Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23247Generated: October 27, 2026

Phosphorus oxide (P4O10) → 3'-O (2-tert-Butyldimethylsilylhydroxyethyl)adenosine

https://huagongshe.com/reaction/23247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantSodium hydrideHCID 24758—
ReactantAdenosineHCID 60961—
Reactant(2-Bromoethyl)-t-butyldimethylsilaneHCID 22592803—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3'-O (2-tert-Butyldimethylsilylhydroxyethyl)adenosineHCID 131723407—

Reaction Steps

Adenosine (10 g, 37.42 mmol) was dried over P2O5 under high vacuum. It was then suspended in anhydrous DMF (150 mL) and NaH (1.35 g, 56.13 mmol) was added. The reaction mixture was stirred at room temperature under inert atmosphere for 30 min. Then (2-bromo ethyl)-tert-butyldimethylsilane (9.68 mL, 4.4.90 mmol) was added dropwise and the reaction mixture stirred at room temperature overnight. DMF was removed under vacuum and to the residue dichloromethane (100 mL) was added and washed with water (2×80 mL). Dichloromethane layer was dried over anhydrous Na2SO4 and evaporated to dryness. Residue purified by column to get a mixture of the title compounds (4.30 g). Rf 0.49, 0.57 (10% MeOH in CH2Cl2)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849723B2
Source datasetuspto-grants-2005_02
ORD IDord-ecad48429eb141fb9aece343ce6fa8fb
Source noteuspto-grants-2005_02