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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333846생성일: 2026년 10월 25일

3-Methoxyphenylhydrazine hydrochloride → (3-Methoxyphenyl)hydrazine

https://huagongshe.com/reaction/333846

반응식

참여 물질

역할이름HCID투입량
반응물3-Methoxyphenylhydrazine hydrochlorideHCID 2723940—
용매Sodium HydroxideHCID 14798—
생성물(3-Methoxyphenyl)hydrazineHCID 423605—

반응 단계

3-Methoxyphenylhydrazine hydrochloride (1 g) was suspended in 1M aqueous NaOH solution and extracted with ether. The organic phase was dried (MgSO4), filtered and concentrated to dryness to give 3-methoxyphenylhydrazine. 2,5-Dibromobenzaldehyde (1 g) and N-methylpyrrolidone (3.7 ml) were added and the mixture was heated under microwave conditions to 160° C. for 10 min. K2CO3 (1.015 g), CuI (36 mg) and trans-N,N′-dimethyl-cyclohexane-1,2-diamine (53 mg) were added and the mixture was heated under microwave conditions to 160° C. for 40 min. CuI (18 mg) and trans-N,N′-dimethyl-cyclohexane-1,2-diamine (26 mg) were added and the mixture was heated under microwave conditions to 160° C. for 20 min. The mixture was filtered and the filtrate was concentrated. The product was purified by chromatography (SiO2, CH2Cl2/MeOH 100:0=>95:5) to give the title compound (659 mg) as a yellow oil. MS (m/e)=303.0 [M+H+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883786B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-d875e1bf69bd4a1495496b99f0e59c92
출처 메모uspto-grants-2014_11