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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41939생성일: 2026년 10월 23일

1-(3-Hydroxy-4-methoxyphenyl)ethanone → 4-[[(E)-1-(3-hydroxy-4-methoxyphenyl)ethylideneamino]oxymethyl]benzonitrile

https://huagongshe.com/ko/reaction/41939

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-Hydroxy-4-methoxyphenyl)ethanoneHCID 95693—
반응물113211-35-1HCID 19692695—
생성물4-[[(E)-1-(3-hydroxy-4-methoxyphenyl)ethylideneamino]oxymethyl]benzonitrileHCID 2510041151%

반응 단계

Acetophenone 12 (30 mg, 0.181 mmol) was condensed with O-(4-cyanobenzyl)hydroxylamine hydrochloride (35) (37 mg, 0.200 mmol) according to the general procedure II-B defined above. After being heated for 3 h the reaction mixture was cooled and the solvent removed under reduced pressure. The ensuing solid was filtered off and washed with cold isopropanol (3.0 mL) to afford the title compound CP30283 (27 mg, 51%) as a white solid, m.p. 125.9-129.7° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536157B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-046a4e99e2c84c21b7473af2469c6e6d
출처 메모uspto-grants-2013_09