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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828786Generated: October 25, 2026

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

https://huagongshe.com/reaction/1828786

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzaldehydeHCID 11158—
ReactantPotassium HydroxideHCID 14797—
ReactantMenthoneHCID 26447—
Reactant6-Isopropyl-3-methyl-2-{4-[(4-propoxy-benzylidene)-amino]-benzylidene}-cyclohexanoneHCID 2851099—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-(4-Amino-benzylidene)-6-isopropyl-3-methyl-cyclohexanoneHCID 5023023—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060723B2
Source datasetuspto-grants-2006_06
ORD IDord-6810f3ece94f451fa569d6e48fb266a4
Source noteuspto-grants-2006_06