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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1741707생성일: 2026년 10월 26일

Triethylamine → 3-[2-Benzyl-1-oxo-1,2-dihydroisoquinolin-6-yl]-acrolein

https://huagongshe.com/reaction/1741707

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Acrolein dimethyl acetalHCID 80145—
반응물Tri-o-tolylphosphineHCID 80271—
반응물2-Benzyl-6-bromo-isoquinolin-1-oneHCID 18963984—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-[2-Benzyl-1-oxo-1,2-dihydroisoquinolin-6-yl]-acroleinHCID 53919284—

반응 단계

A mixture of 2-benzyl-6-bromo-1,2-dihydro-1-oxoisoquinoline (1 g, 3.2 mmol), acrolein dimethyl acetal (2.6 mL, 22.4 mmol), Pd(OAc)2 (15 mg, 0.064 mmol), P(o-tolyl)3 (78 mg, 0.26 mmol) and Et3N (0.5 mL, 3.84 mmol) in DMF (2 mL) is heated in a sealed tube apparatus at 120° for 48 hours. After cooling to room temperature, the reaction mixture is diluted with EtOAc, filtered, washed with saturated NaCl solution, dried over MgSO4 concentrated in vacuo, and the residue is chromatographed (silica gel 1:4 EtOAc/hexane) to yield 3-[2-benzyl-1-oxo-1,2-dihydroisoquinolin-6-yl]-acrolein.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05334600
출처 데이터셋uspto-grants-1994_08
ORD IDord-1b40f671cefb4b60846d5f217aea54db
출처 메모uspto-grants-1994_08