戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 632作成日:2026年10月24日

3-Oxetanamine → N-(4-bromo-3-methoxyphenyl)oxetan-3-amine

https://huagongshe.com/ja/reaction/632

反応式

関与物質

役割名称HCID仕込み量
反応物3-OxetanamineHCID 9833923—
反応物1-Bromo-4-iodo-2-methoxybenzeneHCID 12187202—
試薬Sodium t-butoxideHCID 23676156—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物N-(4-bromo-3-methoxyphenyl)oxetan-3-amineHCID 8285813235.77%

反応条件

温度80 °C

反応手順

A solution of 1-bromo-4-iodo-2-methoxybenzene (0.60 g, 1.92 mmol) dissolved in toluene (15 mL) was treated with oxetan-3-amine (0.140 g, 1.92 mmol), SODIUM TERT-BUTOXIDE (0.221 g, 2.30 mmol), XANTPHOS (0.111 g, 0.19 mmol) and TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.044 g, 0.05 mmol) under nitrogen. The resulting mixture was stirred at 80 °C in a sealed tube for 2 hours. The reaction mixture was diluted with water (10 mL), and extracted with ethyl acetate (3x 20 mL). The organic was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution 0-30% EtOAc in Heptane. Pure fractions were evaporated to dryness to afford N-(4-bromo-3-methoxyphenyl)oxetan-3-amine (0.177 g, 35.8 %) as a beige solid.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-29003fa36fea4ddebef83b29dba29c7c
出典メモ750 AstraZeneca ELN dataset