돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257043생성일: 2026년 10월 26일

Water → 2-[3-(4-Fluorophenyl)-propyl]-6-allyloxy-1-oxo-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/257043

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물1-(3-Bromopropyl)-4-fluorobenzeneHCID 14737133—
반응물6-Allyloxy-1,2,3,4-tetrahydroisoquinolin-1-oneHCID 18963952—
용매DimethylformamideHCID 6228—
생성물2-[3-(4-Fluorophenyl)-propyl]-6-allyloxy-1-oxo-1,2,3,4-tetrahydroisoquinolineHCID 18963930—

반응 단계

To a solution of 6-allyloxy-1-oxo-1,2,3,4-tetrahydroisoquinoline (10.6 g, 52 mmol) and 1-bromo-3-(4-fluorophenyl)-propane (17 g, 78 mmol) and KI (430 mg, 2.6 mmol) in dimethyl formamide (DMF) (125 mL) is added NaH (3.1 g, 78 mmol). After 4 hours the reaction mixture is poured into H2O (500 mL) and the resulting suspension is extracted with EtOAc (3×300 mL). The combined organic extracts are washed with H2O (5×200 mL), saturated NaCl solution (2×200 mL), dried over MgSO4 and concentrated in vacuo. The residue is chromatographed (silica gel, 1:1 EtOAc/hexane) to yield 2-[3-(4-fluorophenyl)-propyl]-6-allyloxy-1-oxo-1,2,3,4-tetrahydroisoquinoline as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05260316
출처 데이터셋uspto-grants-1993_11
ORD IDord-352cb185a94147559b750cc1632d8a6a
출처 메모uspto-grants-1993_11