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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 865335생성일: 2026년 10월 26일

Allyl bromide → 2-allyl-8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one

https://huagongshe.com/reaction/865335

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물Sodium hydrideHCID 24758—
반응물8-Methoxy-2,3,4,5-tetrahydro-benzo[c]azepin-1-oneHCID 11275529—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물2-allyl-8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-oneHCID 2290499883%

반응 단계

A solution of 8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one (10.0 g, 0.052 mol) in N,N-dimethylformamide (30 mL) and allylbromide (23 mL, 0.260 mL) was treated with NaH (60% by wt. dispersion in oil, 2.50 g, 0.063 mol) and the resulting grey suspension stirred at room temperature under an atmosphere of argon. Gas evolution was noted. After 15 minutes, the solution was diluted with brine and partitioned between ethyl acetate and brine. The combined organic layers were concentrated in vacuo and purified by chromatography over silica gel eluting with a gradient of hexane to 1:1 ethyl acetate/hexane to yield 8 g (83%) of 2-allyl-8-methoxy-2,3,4,5-tetrahydro-1H-2-benzazepin-1-one as a colorless oil: 1H NMR(CDCl3) d7.23(m, 1H), 7.03(d, J=9 Hz, 1H), 6.90(dd, J=3, 9 Hz, 1H), 5.91(m, 1H), 5.23(m, 2H), 4.20(d, J=6 Hz, 2H), 3.82(s, 3H), 3.18(t, J=6 Hz, 2H), 2.72(t, J=6 Hz, 2H), 1.96(pentet, J=6 Hz, 2H); 13C NMR(CDCl3) d170.59(CO), 158.42(NCO), 136.88, 133.81, 129.43, 129.35, 129.33, 117.56, 117.54, 112.98, 55.26, 49.43, 45.37, 29.57, 29.22; MS(FAB)m/z=232.1(MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05565449
출처 데이터셋uspto-grants-1996_10
ORD IDord-e6f7f3710ee24f37b0079fd5a8625732
출처 메모uspto-grants-1996_10