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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566586Generated: October 25, 2026

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

https://huagongshe.com/reaction/566586

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 (1 L). After the exothernic 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 (1.5 L) 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 numberUS06175012B1
Source datasetuspto-grants-2001_01
ORD IDord-683561d02eb04facadd8ea712f22925e
Source noteuspto-grants-2001_01