HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746906Generated: October 30, 2026
Ammonium Acetate → HCID 22278884, compound
https://huagongshe.com/reaction/746906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3,5-Diethyl-3-methyl-1-(phenylmethyl)-4-piperidinone | HCID 22278878 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22278884 | HCID 22278884 | — |
Reaction Steps
Ammonium acetate (8.0 g, 104 mmol) was added to the stirred solution of 1-benzyl-3,5-diethyl-3-methyl-4-piperidone (2.5 g, 9.65 mmol) in methanol (25 ml) and stirring was continued for 24 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (0.69 g, 11.2 mmol) was added to it. Cooling was removed after 10 min. and resulting mixture was stirred for 20 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 2) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1M sodium hydroxide solution (pH 9) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to furnish 4-amino-1-benzyl-3,5-diethyl-3-methylpiperidine as an oil. Yield 2.1 g (84%), C17H28N2, m/z 261 (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-d5b122e3ec04406eaa53a14fa3532ac6 |
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| Source note | uspto-grants-2008_07 |
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