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HRID 734824作成日:2026年10月26日

Ethylene Glycol → (4-Bromo-2-methylphenyl)-[2-(4-methylpiperidin-1-yl)ethyl]amine

https://huagongshe.com/reaction/734824

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物2-(4-Methylpiperidin-1-yl)ethan-1-amineHCID 783700—
反応物5-Bromo-2-iodotolueneHCID 2724601—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒IsopropanolHCID 3776—
生成物(4-Bromo-2-methylphenyl)-[2-(4-methylpiperidin-1-yl)ethyl]amineHCID 69054033—

反応手順

5.00 g (35.00 mmol) of 2-(4-methylpiperidin-1-yl)ethylamine was added under argon to a mixture of 10.39 g (35.00 mmol) of 4-bromo-1-iodo-2-methylbenzene, 0.33 g (1.75 mmol) of CuI, 30.0 g (141.00 mmol) of potassium phosphate, and 4.34 g (70.00 mmol) of ethylene glycol in 35 mL of isopropanol and the mixture was refluxed for 15 hours. The reaction mixture was evaporated down in vacuo and the residue taken up in EtOAc. The organic phase was washed with 5% aqueous ammonia, dried over magnesium sulfate, and evaporated down in vacuo. The crude product was purified by column chromatography (silica gel, EtOAc). Yield: 1.20 g (11% of theoretical); C15H23BrN2 (M=311.261); calc.: molpeak (M+H)+: 311/313 (Br); found: molpeak (M+H)+: 311/313 (Br); HPLC-MS: 4.24 minutes (method B).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07592358B2
出典データセットuspto-grants-2009_09
ORD IDord-c3c43faa4ea44b69a685af769a8c04d0
出典メモuspto-grants-2009_09