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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1884263생성일: 2026년 10월 25일

Tetrahydrofuran → N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamide

https://huagongshe.com/reaction/1884263

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물2-(4-Methylphenyl)acetyl chlorideHCID 2760634—
반응물3-Methoxy-4-phenylmethoxyphenylisopropylamineHCID 14579452—
용매WaterHCID 962—
생성물N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamideHCID 2350901470.1%

반응 조건

온도0 °C

반응 단계

2.30 g (8.48 mmol) of crude 2-(4-benzyloxy-3-methoxyphenyl)-1-methylethylamine, 1.03 g (10.2 mmol) of triethylamine and 25 ml of tetrahydrofuran were mixed and cooled to about 0° C. and then 1.42 g (8.48 mmol) of (4-methylphenyl)acetyl chloride was added dropwise thereto. The mixture was stirred at 0° C. for 30 minutes and further at room temperature for 2 hours. Water was added to the reaction mixture, which was followed by extracted with ethyl acetate, washed with 5% hydrochloric acid and saturated brine subsequently, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was washed with hexane and dried to give 2.40 g of N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl) acetamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06762321B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-2db66898ab8045e3b068d5d260c468c6
출처 메모uspto-grants-2004_07