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HRID 566586作成日:2026年10月27日

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

https://huagongshe.com/reaction/566586

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChloropyridineHCID 7977—
反応物(R)-(-)-2-Amino-1-propanolHCID 80308—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-N-(2-pyridyl)-2-aminopropanolHCID 2133942287.4%

反応手順

(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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06175012B1
出典データセットuspto-grants-2001_01
ORD IDord-683561d02eb04facadd8ea712f22925e
出典メモuspto-grants-2001_01