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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11460Generated: October 26, 2026

Ethyl Acetate → 3-(t-Butyldiphenylsilyloxy)-3-(4-pyridyl)propylamine

https://huagongshe.com/reaction/11460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-(t-Butyldiphenylsiloxy)-3-(4-pyridyl)propionitrileHCID 21974219—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3-(t-Butyldiphenylsilyloxy)-3-(4-pyridyl)propylamineHCID 1213664417.8%

Reaction Steps

Lithium aluminum hydride (299 mg, 7.87 mmol) was suspended in anhydrous diethyl ether (10 ml) under a nitrogen atmosphere, and a solution of the obtained 3-(t-butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile (1.00 g, 2.59 mmol) in anhydrous diethyl ether (15 ml) was added dropwise to the suspension under ice-cooling with stirring over eight minutes. The temperature was raised to room temperature, and the mixture was stirred for 75 minutes. The reaction mixture was cooled with ice, ethyl acetate (15 ml) was added to the reaction mixture, and water (0.28 ml), a 15% aqueous sodium hydroxide solution (0.28 ml) and water (0.85 ml) were added thereto successively. The temperature was raised to room temperature, and the whole was stirred for 10 minutes. The reaction mixture was dried over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the titled compound (180.0 mg, yellow oily matter, 17.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098226B2
Source datasetuspto-grants-2006_08
ORD IDord-f849e22082904606b4e01986dc77a519
Source noteuspto-grants-2006_08