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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219571생성일: 2026년 10월 25일

Acetic Acid → 2-Ethyl-1,2,3,4-tetrahydroisoquinoline-7-carbonitrile

https://huagongshe.com/reaction/219571

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AcetaldehydeHCID 177—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물7-Cyano-1,2,3,4-tetrahydroisoquinolineHCID 10176243—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-Ethyl-1,2,3,4-tetrahydroisoquinoline-7-carbonitrileHCID 59746352—

반응 단계

To a solution of 1,2,3,4-tetrahydroisoquinoline-7-carbonitrile (ABCR; 500 mg; 3.16 mmol) in MeOH (5 mL) at 0° C. was added acetaldehyde (0.51 mL, 8.91 mmol) and acetic acid (5 μL) and the resulting mixture was stirred for 1 hour. Sodium cyanoborohydride (218 mg; 3.47 mmol) was added and the mixture was stirred for 5 hours and diluted with DCM (100 mL) and water (20 mL). The aqueous layer was extracted with DCM (3×20 mL), the combined organics were dried (MgSO4) and the solvent was removed in vacuo. The residue was purified by flash chromatography on a Biotage 25+M column, eluting with petrol containing increasing amounts of EtOAc to give the title compound as a brown oil. 1H NMR: (CDCl3, 400 MHz) δ 7.39 (1H, d, J=8.0 Hz), 7.33 (1H, s), 7.19 (1H, d, J=8.0 Hz), 3.62 (2H, s), 2.99-2.90 (2H, m), 2.77-2.70 (2H, m), 2.66-2.54 (2H, m), 1.19 (3H, t, J=7.2 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202856B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-9004fde4d0c04ff7988142e08b0c501d
출처 메모uspto-grants-2012_06