戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1662736作成日:2026年10月24日

Morpholine → 4-(3-Bromo-4-methoxyphenyl)morpholine

https://huagongshe.com/ja/reaction/1662736

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物Tris(1,1-dimethylethyl)phosphineHCID 83681—
反応物2-Bromo-4-iodoanisoleHCID 3376779—
反応物Sodium t-butoxideHCID 23676156—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物4-(3-Bromo-4-methoxyphenyl)morpholineHCID 67429791—

反応条件

温度45 °C

反応手順

Under nitrogen atmosphere, to a solution of 20.0 g of 2-bromo-4-iodoanisole in toluene (250 ml) was added morpholine (6.12 ml), 1.29 g of tri-tert-butyl phosphine, 13.5 g of sodium tert-butoxide, and 359 mg of palladium acetate (II), and the reaction mixture was stirred for two hours at 45° C. Water and EtOAc were added to the reaction solution, liquid separation was performed and the aqueous layer was extracted with EtOAc. The combined organic layer was washed with saturated brine, dried over MgSO4, then, the drying agent was separated by filtration, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography (Chromatorex NH; mobile phase: n-hexane/EtOAc=10/1 to 3/1; v/v) to obtain 3.94 g of the title compound (colorless powder).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030499B2
出典データセットuspto-grants-2011_10
ORD IDord-ed2204e738f3451d964cad9d09492659
出典メモuspto-grants-2011_10