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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884568Generated: October 27, 2026

Ethylene Oxide → 3-(3-Cyanopyridin-4-yl)-1-propanol

https://huagongshe.com/reaction/1884568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantDiisopropylamineHCID 7912—
ReactantHexaneHCID 8058—
Reactant4-Methyl-3-cyanopyridineHCID 227806—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Cyanopyridin-4-yl)-1-propanolHCID 2350621337%

Reaction Conditions

Temperature20 °C

Reaction Steps

Diisopropylamine (2.5 g, 25 mmol) is dissolved in THF (30 ml), and thereto is added a solution of n-butyl lithium in hexane (14.3 ml, 24 mmol) at −70° C. The mixture is stirred for 15 minutes, and thereto is added a solution of 3-cyano-4-methylpyridine (2.4 g, 20 mmol) obtained in Reference Example 33 in THF (20 ml). Ten minutes thereafter, ethylene oxide (1.1 g, 24 mmol) is added to the mixture, and the mixture is warmed to 20° C. over a period of time for one hour. The reaction is quenched with a saturated brine (50 ml), and the mixture is extracted with ethyl acetate (150 ml×2). The organic layer is washed with a saturated brine (100 ml×2), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to give the title compound (1.2 g) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06765095B2
Source datasetuspto-grants-2004_07
ORD IDord-e923d8275ae84c76895826e506133f03
Source noteuspto-grants-2004_07