HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85292Generated: October 26, 2026
Isophorone → 3-[2-(4-Dibutylamino-2-methoxyphenyl)vinyl]-5,5-dimethyl-2-cyclohexenone
https://huagongshe.com/reaction/85292
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isophorone | HCID 6544 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-(Dibutylamino)-2-methoxybenzaldehyde | HCID 14643903 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[2-(4-Dibutylamino-2-methoxyphenyl)vinyl]-5,5-dimethyl-2-cyclohexenone | HCID 68008965 | 45% |
Reaction Steps
In 15 ml of tetrahydrofuran, 1.5 g (10.85 mmol) of isophorone was dissolved, and 3.4 g of sodium ethoxide (20% solution in ethanol) (10.0 mmol) was added thereto. To this mixture, 2.6 g (9.87 mmol) of 4-dibutylamino-2-methoxybenzaldehyde in tetrahydrofuran was added dropwise with heating at 50° C., and the mixture was stirred for 4.5 hours. To the mixture, 100 ml of ethyl acetate was added. Washing with a saturated saline solution, drying over anhydrous sodium sulfate, and concentration were performed. The residue was purified by silica gel column chromatography to give 1.7 g of a reddish orange oily matter (yield: 45.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846955B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-19e301df09d24f28bc8d5a9e1c5a6ef8 |
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| Source note | uspto-grants-2014_09 |
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