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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11459Generated: October 25, 2026

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

https://huagongshe.com/reaction/11459

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 further stirred at an external temperature of 50° C. for three hours. Ethyl acetate (50 ml) and ether (50 ml) were added to the reaction mixture, the whole was washed with water (20 ml) three times and saturated brine (30 ml) successively, and the organic layer was dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give 2.58 g (98.9%) of 3-(t-butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile as a colorless oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098226B2
Source datasetuspto-grants-2006_08
ORD IDord-5796659c7f674d9aaacb6e64badd6d98
Source noteuspto-grants-2006_08