HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063299Generated: October 30, 2026
Ethylamine hydrochloride → HCID 22278836, compound
https://huagongshe.com/reaction/1063299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-Benzyl-3,3-dimethylpiperidin-4-one | HCID 9794413 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22278836 | HCID 22278836 | — |
Reaction Steps
Potassium hydroxide (4.6 g, 83.0 mmol) was added to the stirred solution of ethylamine hydrochloride (6.8 g, 83.0 mmol) in methanol (70 ml) and stirring was continued for 30 min at 30° C. 1-benzyl-3,3-dimethyl-4-piperidone (3.5 g, 16.6 mmol)), was added to the resulting mixture and stirred for 6 hr. Sodium cyanoborohydride (1.0 g, 16.6 mmol) was added to it and reaction mixture was stirred for 15 hr. The reaction mixture was concentrated to dryness, triturated with water, extracted with chloroform, dried (Na2SO4) and concentrated to give 1-benzyl-4-ethylamino-3,3-dimethylpiperidine. Yield 3.8 g (88%), C16H26N2, m/z 247 (M+1), PMR (CDCl3): 0.9 (s, 3H), 1.06 (s, 3H), 1.18-1.38 (m, 5H), 1.64-2.8 (m, 6H), 2.94 (m, 1H), 3.44 (dd, 2H), 7.2 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06964966B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-abb244ae254b4318860ada1fc60dfd2c |
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| Source note | uspto-grants-2005_11 |
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