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HRID 22183생성일: 2026년 10월 23일

6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one → 6-Amino-5-methyl-2-ethoxy-3,1-benzoxazin-4-one

https://huagongshe.com/ko/reaction/22183

반응식

참여 물질

역할이름HCID투입량
반응물6-Nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-oneHCID 15283173—
촉매PalladiumHCID 23938—
용매Ethyl AcetateHCID 8857—
생성물6-Amino-5-methyl-2-ethoxy-3,1-benzoxazin-4-oneHCID 1528317471%

반응 단계

A solution of 4.0 g (16 mmoles) of 6-nitro-5-methyl-2-ethoxy-3,1-benzoxazin-4-one in 65 mL ethyl acetate was transferred to a Parr bottle. 1.0 g (0.94 mmoles) 10% Pd/C catalyst (obtained from Matheson, Coleman & Bell) was added. The sample was hydrogenated on a Parr shaker at ambient room temperature and 1 atm pressure for 5 hours. The catalyst was removed by filtration through a pad of Celite. The filtrate was concentrated in vacuo to produce a bright yellow solid. There was obtained 2.5 g (71% yield) of 6-amino-5-methyl-2-ethoxy-3,1-benzoxazin-4-one. NMR (DMSO-d6): 1.33(t,3H,J=6.9 Hz), 2.46(s,3H), 4.36(q,2H,J=6.9 Hz), 5.24(bs,2H), 7.05(d,1H,J=8.4 Hz), 7.14(d,1H,J=8.4 Hz). IR(nujol): 1743 cm-1 (lactone carbonyl). MS(m/z): 220(M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428021
출처 데이터셋uspto-grants-1995_06
ORD IDord-3e8b6797605a414c915acc79bb35d696
출처 메모uspto-grants-1995_06