HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905143Generated: October 25, 2026
Potassium Hydroxide → 3-(2-Ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenone
https://huagongshe.com/reaction/905143
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Ethylhexanoyl chloride | HCID 79103 | — |
| Reactant | 2-(2',5'-Dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedione | HCID 12876602 | — |
| Catalyst | Dicyclohexano-18-crown-6 | HCID 85955 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(2-Ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenone | HCID 20206510 | 92.3% |
Reaction Steps
A suspension of 1.50 g (6.14 mmol) of 2-(2',5'-dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedione in 15 ml of dry benzene was prepared and 0.49 g (7.37 mmol) of 85% powdered potassium hydroxide was added, followed by 1 drop of dicyclohexyl-18-crown-6-ether. After stirring for 30 minutes, 1.20 g (7.37 mmol) of 2-ethylhexanoyl chloride was added, and the reaction mixture refluxed for 12 hrs. The reaction mixture was cooled to room temperature, taken up in 150 ml ether and 50 ml of water, washed three times with 0.25 N, NaOH, two times with water, two times with 6 N HCl, and once more with water. The ether solution was dried and stripped to leave 2.10 g (92% yield) of 3-(2-ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexenone as a clear, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04422870 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-d9aa4d897b7a423a83ed962dfc0becdd |
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| Source note | uspto-grants-1983_12 |
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