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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18399Generated: October 26, 2026

Imidazole → 3-(t-Butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile

https://huagongshe.com/reaction/18399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant3-Hydroxy-3-(pyridin-4-yl)propanenitrileHCID 21973939—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product3-(t-Butyldiphenylsiloxy)-3-(4-pyridyl)propionitrileHCID 2197421998.9%

Reaction Steps

Next, imidazole (4.60 g, 67.5 mmol) and N,N-dimethylformamide (30 ml) were added to the obtained 3-hydroxy-3-(4-pyridyl)propionitrile (1.00 g, 6.75 mmol), and the mixture was stirred at room temperature. t-Butyldiphenylchlorosilane (2.23 g, 8.10 mmol) was added to the mixture, and the whole was stirred for one day and then stirred further at an external temperature of 50° C. for three hours. Ethyl acetate (50 ml) and ether (50 ml) were added thereto, and the whole was washed with water (20 ml) three times and saturated brine (30 ml) successively. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 3-(t-butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile (2.58 g, 98.9%) as a colorless oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741346B2
Source datasetuspto-grants-2010_06
ORD IDord-1afb9fe9375140518b7d7d258c08a4b4
Source noteuspto-grants-2010_06