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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501884Generated: October 30, 2026

Pyridine → HCID 21729362, compound

https://huagongshe.com/reaction/501884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 10055554HCID 10055554—
CatalystSilver NitrateHCID 24470—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21729362HCID 2172936284.8%

Reaction Steps

Anhydrous pyridine (9.9 mL) was added to a solution of 5′-O-(4,4′-dimethoxitrityl)-5-methyluridine (6.9 g) and AgNO3 (2.51 g) in dry THF (123 mL) and stirred at room temperature for 20 min under an argon atmosphere. Followed by addition of tert-butyldimethylsilyl chloride (2.51 g) in dry THF (6 mL) and stirred at the same temperature for 2-3 h. The solids were filtered off and the filtrate was concentrated to a crude residue which was applied to a column of silica gel eluted with hexane-ethyl acetate (3:1) to give a pure title compound (7.04 g) as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772387B2
Source datasetuspto-grants-2010_08
ORD IDord-18574bf0ec8341f898f8ff741ba41d56
Source noteuspto-grants-2010_08