HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980908Generated: October 30, 2026
Diisopropylamine → 2-Acetyl-4-(4-pyridyl)cyclohexanone
https://huagongshe.com/reaction/980908
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Acetylimidazole | HCID 538972 | — |
| Reactant | Cyclohexanone, 4-(4-pyridinyl)- | HCID 10154273 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Acetyl-4-(4-pyridyl)cyclohexanone | HCID 13772055 | 66.5% |
Reaction Steps
To a solution of 3.2 ml of diisopropylamine dissolved in 40 ml of tetrahydrofuran, there was added 14.2 ml of 1.6M solution of n-butyl lithium in hexane at -20° C. Then, a solution of 2 g of 4-(4-pyridyl)cyclohexanone dissolved in 40 ml of tetrahydrofuran was added at -40° C. The reaction mixture was cooled to -78° C., and 2.5 g of acetylimidazole dissolved in 40 ml of tetrahydrofuran was added. The reaction mixture was stirred at room temperature, poured into ice water, and then washed with ether. The aqueous layer was saturated with ammonium chloride and extracted with methylene chloride. Thus, there was obtained 1.65 g of 2-acetyl-4-(4-pyridyl)cyclohexanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04639521 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-0db94c5d2858435699da62e6e0524781 |
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| Source note | uspto-grants-1987_01 |
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