HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8701Generated: October 24, 2026
Acetic Acid → 1-benzyl-N,4-dimethylpiperidin-3-amine
https://huagongshe.com/en/reaction/8701
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 1-Benzyl-4-methylpiperidin-3-one | HCID 12084828 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-benzyl-N,4-dimethylpiperidin-3-amine | HCID 9943889 | 69% |
Reaction Steps
To a stirred solution of 1-benzyl-4-methyl-piperidin-3-one (2.3 grams, 11.5 mmol), prepared by the methods of Iorio, M. A. and Damia, G., Tetrahedron, 26, 5519 (1970) and Grieco et al., Journal of the American Chemical Society, 107, 1768 (1985), (modified using 5% methanol as a co-solvent), both references are incorporated by reference in their entirety, dissolved in 23 mL of 2 M methylamine in tetrahydrofuran was added 1.4 mL (23 mmol) of acetic acid and the resulting mixture stirred in a sealed tube for 16 hours at room temperature. Triacetoxy sodium borohydride (4.9 grams, 23 mmol) was added and the new mixture stirred at room temperature in a sealed tube for 24 h, at which time, the reaction was quenched upon addition of 1 N sodium hydroxide (50 mL). The reaction mixture was then extracted 3×80 mL with ether, the combined ether layers dried over sodium sulfate (Na2SO4) and concentrated to dryness in vacuo affording 1.7 grams (69%) of the title compound as a white solid. LRMS: 219.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07091208B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-8210397d84ee46a398b1d1f423bf0696 |
|---|
| Source note | uspto-grants-2006_08 |
|---|