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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937726Generated: October 23, 2026

2-Chloropyridine → (R)-N-(2-pyridyl)-2-aminopropanol

https://huagongshe.com/en/reaction/1937726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyridineHCID 7977—
Reactant(R)-(-)-2-Amino-1-propanolHCID 80308—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product(R)-N-(2-pyridyl)-2-aminopropanolHCID 2133942287.4%

Reaction Steps

(R)-Alaninol (107.3 g, 1.43M) was added dropwise with stirring to a solution of potassium tertiary butoxide (160 g, 1.43M) in tetrahydrofuran (1L). After the exothermic reaction had cooled to room termperature, 2-chloropyridine (162.4 g, 1.43M) was added dropwise. The reaction mixture was heated under reflux overnight, cooled, filtered and evaporated to an oil. The oil was dissolved in xylene (1,5L) and toluene-p-sulphonic acid (0.5 g) was added. The mixture was heated under reflux overnight. On cooling to room temperature the product crystallised to give (R)-N-(2-pyridyl)-2-aminopropanol (190 g), [α]D26=30° (c=1 in CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395902B1
Source datasetuspto-grants-2002_05
ORD IDord-567d0f352f694ca785f48c23cb95f136
Source noteuspto-grants-2002_05