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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminobenzaldehyde | HCID 11158 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Menthone | HCID 26447 | — |
| Reactant | 6-Isopropyl-3-methyl-2-{4-[(4-propoxy-benzylidene)-amino]-benzylidene}-cyclohexanone | HCID 2851099 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Amino-benzylidene)-6-isopropyl-3-methyl-cyclohexanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07060723B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-6810f3ece94f451fa569d6e48fb266a4 |
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| Source note | uspto-grants-2006_06 |
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