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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352002Generated: October 28, 2026

Imidazole → HCID 22878626, compound

https://huagongshe.com/reaction/352002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 54519329HCID 54519329—
SolventPyridineHCID 1049—
ProductHCID 22878626HCID 22878626—

Reaction Steps

1′-Cyano-5′-(4,4′-dimethoxytrityl)thymidine in anhydrous pyridine is added to a stirred solution of t-butyldimethylchlorosilane (1.5 equivalents) and imidazole (3.0 equivalents) in anhydrous pyridine at 0° C. The resulting reaction mixture is stirred at room temperature overnight. Pyridine is evaporated and the residue dissolved in ethyl acetate, washed with brine. The crude is directly used for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743902B1
Source datasetuspto-grants-2004_06
ORD IDord-ae53bcb2af1142f6a29a4bbd291a8c07
Source noteuspto-grants-2004_06