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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379878Generated: October 30, 2026

Imidazole → 4-(Tert-butyldimethylsilyloxymethyl)pyridinecarbonitrile

https://huagongshe.com/reaction/379878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-(Hydroxymethyl)pyridine-2-carbonitrileHCID 10725391—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-(Tert-butyldimethylsilyloxymethyl)pyridinecarbonitrileHCID 14541448—

Reaction Steps

To a solution of 2-cyano-4-hydroxymethylpyridine (step 1, 3.63 g, 27.06 mmol) in DMF (50 ml) were added imidazole (4.42 g, 64.95 mmol) and TBDMSCl (4.89 g, 32.47 mmol) at room temperature. After stirring for 1 h, the mixture was diluted with diethyl ether (300 ml), washed with water (100 ml×4), and dried (MgSO4). Removal of solvent gave the title compound. 1H-NMR (CDCl3) δ: 8.65 (1 H, d, J=5.1 Hz), 7.68 (1 H, s), 7.46 (1 H, d, J=4.9 Hz), 4.78 (2 H, s), 0.96 (9 H, s), 0.13 (6 H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300363B1
Source datasetuspto-grants-2001_10
ORD IDord-483f7f8762f54b97b11ec9611bc15893
Source noteuspto-grants-2001_10