戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 82904作成日:2026年10月27日

Bromine → 2-Amino-5-bromo-3-(hydroxymethyl)pyridine

https://huagongshe.com/reaction/82904

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物(2-Aminopyridin-3-yl)methanolHCID 11159325—
溶媒Acetic AcidHCID 176—
生成物2-Amino-5-bromo-3-(hydroxymethyl)pyridineHCID 10891366—

反応手順

Bromine (10.4 mL, 202 mmol) was added dropwise over 1 hour to a solution of 2-amino-3-(hydroxymethyl)pyridine (25.1 g, 202 mmol) in acetic acid (500 mL) at room temperature. After complete addition the reaction mixture was stirred for an extra hour. After concentration to dryness, the residue was partitioned between 1M Na2CO3 (750 mL) and ethyl acetate (500 mL). The aqueous layer was separated and extracted one more time with ethyl acetate (500 mL). The combined organic phases were washed with a saturated solution of sodium chloride (500 mL), dried over sodium sulfate, filtered and concentrated to dryness. After trituration of the residue in DCM/heptane and extra washing with DCM the title product was obtained as a light yellow solid (30.0 g, 70%, py 97.3%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846711B2
出典データセットuspto-grants-2014_09
ORD IDord-3a86a9eaded740f2b1c5892377322a6d
出典メモuspto-grants-2014_09