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HRID 2305713作成日:2026年10月24日

Ammonia → 5-(Benzyloxy)pyridin-3-amine

https://huagongshe.com/ja/reaction/2305713

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物3-(Benzyloxy)-5-bromopyridineHCID 15389198—
触媒Copper sulfate pentahydrateHCID 24463—
生成物5-(Benzyloxy)pyridin-3-amineHCID 22989735—

反応条件

温度180 °C

反応手順

A thick-walled glass pressure tube was charged with copper(II) sulfate pentahydrate (1.96 g, 7.85 mmol), 5-bromo-3-(phenylmethoxy)pyridine (4.00 g, 15.15 mmol) and concentrated aqueous ammonia (29.7%, 14.8 M, 37 mL). The tube was sealed and the dark blue suspension was stirred and heated at 180° C. (oil bath temperature) for 24 h. The mixture was allowed to cool to ambient temperature. After further cooling in an ice-water bath, the mixture was concentrated on a rotary evaporator to a small volume (˜20 mL) of a dark-blue solution. The solution was diluted with water (40 mL) and saturated K2CO3 solution (40 mL) and extracted with CHCl3 (4×40 mL). The combined, turbid-brown CHCl3 extracts were washed with saturated NaCl solution (2×100 ml), dried (Na2SO4), filtered and concentrated (rotary evaporator). The resulting dark-brown oil, was briefly dried on the vacuum pump to give a dark-brown solid (2.06 g). The product was purified by column chromatography on silica gel (100 g) eluting with CHCl3—MeOH (3:1, v/v). Selected fractions, based on TLC (Rf 0.65) analysis, were combined and concentrated to give a 1.64 g (54.1%) of a tan-brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06441006B2
出典データセットuspto-grants-2002_08
ORD IDord-6d8b956597844218b402c3ea67f8942a
出典メモuspto-grants-2002_08