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HRID 12935作成日:2026年10月23日

4-Aminobenzaldehyde → 2-(4-Amino-benzylidene)-6-isopropyl-3-methyl-cyclohexanone

https://huagongshe.com/ja/reaction/12935

反応式

関与物質

役割名称HCID仕込み量
反応物4-AminobenzaldehydeHCID 11158—
反応物Potassium HydroxideHCID 14797—
反応物MenthoneHCID 26447—
反応物6-Isopropyl-3-methyl-2-{4-[(4-propoxy-benzylidene)-amino]-benzylidene}-cyclohexanoneHCID 2851099—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物2-(4-Amino-benzylidene)-6-isopropyl-3-methyl-cyclohexanoneHCID 5023023—

反応手順

A compound having general Formula 3, exemplified by 6-Isopropyl-3-methyl-2-{4-[(4-propoxy-benzylidene)-amino]-benzylidene}-cyclohexanone (Compound 3; FIG. 1) can be prepared as follows. A solution of menthone (154 mg, 1.0 mmol) and 4-aminobenzaldehyde (121 mg, 1.0 mmol) in dimethylsulfoxide is treated with potassium hydroxide (56 mg, 1.0 mmol). The reaction is stirred until no futher reaction occurs. The reaction mixture is poured into ethyl acetate and water. The organic phase is collected, dried and concentrated to give 2-(4-Amino-benzylidene)-6-isopropyl-3-methyl-cyclohexanone. The 2-(4-Amino-benzylidene)-6-isopropyl-3-methyl-cyclohexanone is dissolved in dichloromethane and treated with 4-propoxybenzaldehyde (164 mg, 1.0 mmol) and anhydrous Na2SO4. The reaction mixture is stirred until no further reaction occurs. The reaction mixture is filtered and concentrated to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728034B2
出典データセットuspto-grants-2010_06
ORD IDord-36bc0f6536184b72bdf9a287f7b6fe07
出典メモuspto-grants-2010_06