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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12935생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물4-AminobenzaldehydeHCID 11158—
반응물Potassium HydroxideHCID 14797—
반응물MenthoneHCID 26447—
반응물6-Isopropyl-3-methyl-2-{4-[(4-propoxy-benzylidene)-amino]-benzylidene}-cyclohexanoneHCID 2851099—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(4-Amino-benzylidene)-6-isopropyl-3-methyl-cyclohexanoneHCID 5023023—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728034B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-36bc0f6536184b72bdf9a287f7b6fe07
출처 메모uspto-grants-2010_06