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HRID 333846作成日:2026年10月26日

3-Methoxyphenylhydrazine hydrochloride → (3-Methoxyphenyl)hydrazine

https://huagongshe.com/reaction/333846

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methoxyphenylhydrazine hydrochlorideHCID 2723940—
溶媒Sodium HydroxideHCID 14798—
生成物(3-Methoxyphenyl)hydrazineHCID 423605—

反応手順

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+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883786B2
出典データセットuspto-grants-2014_11
ORD IDord-d875e1bf69bd4a1495496b99f0e59c92
出典メモuspto-grants-2014_11