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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41933생성일: 2026년 10월 23일

Acetovanillone → 2-methoxy-4-[(E)-C-methyl-N-[(4-nitrophenyl)methoxy]carbonimidoyl]phenol

https://huagongshe.com/ko/reaction/41933

반응식

참여 물질

역할이름HCID투입량
반응물AcetovanilloneHCID 2214—
반응물Hydroxylamine, O-((4-nitrophenyl)methyl)-, hydrochloride (1:1)HCID 74967—
생성물2-methoxy-4-[(E)-C-methyl-N-[(4-nitrophenyl)methoxy]carbonimidoyl]phenolHCID 13592372555.3%

반응 단계

4′-Hydroxy-3′-methoxyacetophenone (25) (150 mg, 0.903 mmol) was condensed with compound 19 (0.203 g, 0.992 mmol) according to the general procedure II-A defined above. After being heated for 3 h the reaction mixture was cooled and the solvent removed under reduced pressure. The ensuing residue was dissolved in CH2Cl2 (20 mL), washed with H2O (2×15 mL) then dried (MgSO4), filtered and concentrated under reduced pressure. The residue thus obtained was subjected to flash chromatography (1:9 v/v ethyl acetate/hexane elution) to afford the title compound CP30261 (158 mg, 55%) as a yellow solid, m.p. 118.4-121.1° C., Rf 0.5 in 1:1 v/v ethyl acetate/hexane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536157B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-7eae7d2e5e7f4229acacea5a3aec6b6e
출처 메모uspto-grants-2013_09