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HRID 516964作成日:2026年10月23日

Dichloromethane → 4-(4-Bromo-3-fluorobenzyl)morpholine

https://huagongshe.com/ja/reaction/516964

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物MorpholineHCID 8083—
反応物4-Bromo-3-fluorobenzaldehydeHCID 2783411—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
溶媒Dichloromethane methanolHCID 21226129—
生成物AmmoniaHCID 222—
生成物4-(4-Bromo-3-fluorobenzyl)morpholineHCID 5341781866%

反応条件

温度59 °C

反応手順

A mixture of morpholine (0.215 ml, 2.46 mmol) and 4-bromo-3-fluorobenzaldehyde, available from Alfa Aesar, (500 mg, 2.46 mmol) was prepared in chloroform (8 ml) at room temperature and heated to 58-60° C. in a sealed tube for 1 h. The mixture was then cooled to room temperature and sodium triacetoxyborohydride (783 mg, 3.69 mmol) was added and the mixture heated again to 58-60° C. in a sealed tube for 12 h. The mixture was then allowed to cool to room temperature, diluted with water (4 ml), shaken vigorously and the mixture filtered through a phase separator and the filtrate concentrated in vacuo. The mixture was then purified by SCX-2 chromatography (Eluent: dichloromethane (2×10 ml), 10% methanol/dichloromethane (2×10 ml), methanol (2×10 ml), 7M NH3 in methanol/dichloromethane (2×10 ml) to afford 4-(4-bromo-3-fluorobenzyl)morpholine as a colourless oil (447 mg, 1.63 mmol, 66%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115088B2
出典データセットuspto-grants-2015_08
ORD IDord-b04c39a32f78474e804a11fcc2e8dc71
出典メモuspto-grants-2015_08