HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367889Generated: October 25, 2026
Triethylamine → 1-Dimethylamino-piperidin-4-one oxime
https://huagongshe.com/reaction/2367889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 1-(Dimethylamino)-4-piperidinone | HCID 56737782 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Dimethylamino-piperidin-4-one oxime | HCID 86671304 | 68.3% |
Reaction Steps
19.2 g 1-Dimethylamino-piperidin-4-one (prepared as described in Journal of Medicinal & Pharmaceutical Chemistry, 4, 423-36; 1961) and 30 g triethylamine are dissolved in 80 ml methanol. 18.8 g hydroxylamin hydrochloride is added in portions at ambient temperature. The internal temperature raises during the addition to 37° C. Then the mixture is heated to reflux for 3 hours, allowed to cool to room temperature, and then the solvent evaporated. The residue is partitioned between ethyl acetate and aqueous sodium bicarbonate. The organic layer is dried over sodium sulfate, and the solvent evaporated. Thus, 14.5 g 1-Dimethylamino-piperidin-4-one oxime is obtained. 1H-NMR (CDCl3): 8.10 ppm (s, broad, 1H), 2.75 ppm (m, 6H), 2.40 ppm (m, 2H), 2.40 ppm (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703165B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-26a3a45656db442682014dd6ec817748 |
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| Source note | uspto-grants-2014_04 |
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