HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746896Generated: October 25, 2026
Ethylamine hydrochloride → 4-Ethylamino-1-carbethoxy-3,5-dimethylpiperidine
https://huagongshe.com/reaction/746896
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 | 1-Carbethoxy-3,5-dimethyl-4-piperidinone | HCID 22278887 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Ethylamino-1-carbethoxy-3,5-dimethylpiperidine | HCID 22278905 | — |
Reaction Steps
Powdered KOH (2.8 g, 50 mmol) was added in portions to the stirred solution of ethylamine hydrochloride (4.0 g, 50 mmol) in methanol (50 ml) and 1-carbethoxy-3,5-dimethyl-4-piperidinone (5.0 g, 25.12 mmol) obtained by a procedure as described in Example 25 (Step-1), was added to it. The resulting reaction mixture was stirred for 6 hr. A solution of sodium cyanoborohydride (1.6 g, 25.12 mmol) in methanol (10 ml) was added dropwise to it and stirring was continued for 16 hr. The reaction mixture was concentrated to dryness. The obtained residue was dissolved in water and extracted with chloroform. Chloroform layer was extracted with 50% HCl and acid layer was basified with KOH (20%) solution. The oil thus separated was extracted with chloroform, dried (Na2SO4) and concentrated to give Mixtures A+B of 4-ethylamino-1-carbethoxy-3,5-dimethylpiperidine as an oil. Yield 5.6 g (97.7%), C12H24N2O2, m/z 229 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07393957B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-b6c75eaef19b4011bfa22f2693602066 |
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| Source note | uspto-grants-2008_07 |
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