HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865225Generated: October 31, 2026
Ethylamine hydrochloride → 1-Carbethoxy-4-ethylamino-3-methylpiperidine
https://huagongshe.com/reaction/1865225
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Ethyl 3-methyl-4-oxopiperidine-1-carboxylate | HCID 15075657 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Carbethoxy-4-ethylamino-3-methylpiperidine | HCID 22278900 | — |
Reaction Steps
Ethylamine hydrochloride (5 g, 61.34 mmol) was added to the stirred solution of 1-carbethoxy-3-methyl-4-piperidone (3.5 g, 18.9 mmol) obtained as described in Preparation 1, in methanol (30 ml) followed by 3.43 g (61.34 mmol) KOH. Stirring was continued for 3 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (1.4 g, 22.22 mmol) was added to it. Cooling was removed after 10 min. and resulting mixture was stirred for 16 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 3˜4) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1 M sodium hydroxide solution (pH˜10) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to give 1-carbethoxy-4-ethylamino-3-methylpiperidine. Yield 2.3 g (54%), C11H22N2O2, m/z 215 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07626032B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-f4fec2eaadf041a4af7fd5112811f650 |
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| Source note | uspto-grants-2009_12 |
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