HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374341Generated: October 29, 2026
Potassium Carbonate → 2-Acetyl-2-[2-(tert-butoxycarbonyl)ethyl]cyclohexanone
https://huagongshe.com/reaction/374341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Acetylcyclohexanone | HCID 13400 | — |
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Acetyl-2-[2-(tert-butoxycarbonyl)ethyl]cyclohexanone | HCID 10989276 | — |
Reaction Steps
To a suspension of 2-acetylcyclohexanone (100 g, 0.71 mol), potassium carbonate (118.3 g, 0.85 mol) and benzyltriethylammonium chloride (3.18 g, 0.014 mol) in toluene (280 ml), was added, in one portion, tert-butyl acrylate (137.1 g, 155.2 ml, 1.07 mol) at room temperature. The suspension was stirred at 40° C. for 18 hours, diluted with distilled water (1 L) and toluene (500 ml), and the layers separated. The aqueous layer was extracted with toluene (3×500 ml), the combined toluene extracts dried over magnesium sulphate, filtered and concentrated under reduced pressure to give a brown oil, (197.8 g) Rf. 0.41 (silica, hexane/ethyl acetate, 3:1). The crude product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166406 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-820442fe3b7f44158fef658ddfdab54d |
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| Source note | uspto-grants-1992_11 |
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