HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552326Generated: October 31, 2026
Triethylamine → 1-(2-Ethylbutyryl)piperidin-4-one
https://huagongshe.com/reaction/552326
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Ethylbutyryl chloride | HCID 75954 | — |
| Reactant | Piperidin-2-one--hydrogen chloride (1/1) | HCID 20088740 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Ethylbutyryl)piperidin-4-one | HCID 24710387 | — |
Reaction Steps
Triethylamine (5.8 g, 57.3 mmol) and a catalytic amount of DMAP were added to a solution of piperidone hydrochloride (4.0 g, 26 mmol) in CH2Cl2 (20 ml). After cooling to −10° C., 2-ethylbutyryl chloride (3.9 g, 28.6 mmol) dissolved in CH2Cl2 (10 ml) was slowly added and the mixture was stirred at RT for 16 h. 5M potassium hydroxide solution (25 ml) was added to the suspension, the organic phase was separated off and the aqueous phase was extracted with CH2Cl2 (3×10 ml). After drying of the combined organic phases over Na2SO4, filtration and removal of the solvent, the product 1-(2-ethylbutyryl)piperidin-4-one was obtained in a yield of 4.3 g (84% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951815B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-d8be83b15251499db356120b356c60bd |
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| Source note | uspto-grants-2011_05 |
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