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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 734824생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/734824

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-(4-Methylpiperidin-1-yl)ethan-1-amineHCID 783700—
반응물5-Bromo-2-iodotolueneHCID 2724601—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매IsopropanolHCID 3776—
생성물(4-Bromo-2-methylphenyl)-[2-(4-methylpiperidin-1-yl)ethyl]amineHCID 69054033—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07592358B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-c3c43faa4ea44b69a685af769a8c04d0
출처 메모uspto-grants-2009_09