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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1246007생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1246007

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 further 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 번호US07125908B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-a31e71f513f145ae8fcdc7ebee109738
출처 메모uspto-grants-2006_10