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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1884253생성일: 2026년 10월 26일

Tetrahydrofuran → N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-(5,6,7,8-tetrahydronaphthalen-2-yl)acetamide

https://huagongshe.com/reaction/1884253

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물Phenethylamine, 4-(benzyloxy)-3-methoxy-HCID 200382—
반응물(5,6,7,8-Tetrahydronaphthalen-2-yl)acetyl chlorideHCID 23508965—
용매WaterHCID 962—
생성물N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-(5,6,7,8-tetrahydronaphthalen-2-yl)acetamideHCID 23509023—

반응 조건

온도0 °C

반응 단계

8.01 g (31.2 mmol) of crude 2-(3-methoxy-4-benzyloxyphenyl)ethylamine, 3.78 g (37.4 mmol) of triethylamine and 80 ml of tetrahydrofuran were mixed and cooled to 0° C. and then (5,6,7,8-tetrahydronaphthalen-2-yl)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 then saturated brine, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (eluent, hexane:ethyl acetate=1:1) to give 8.3 g of N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-(5,6,7,8-tetrahydronaphthalen-2-yl)acetamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06762321B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-b9be2b3a757c49ffa25f02056c42ac50
출처 메모uspto-grants-2004_07