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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantMethylamineHCID 6329—
Reactant1-Benzyl-4-methylpiperidin-3-oneHCID 12084828—
SolventTetrahydrofuranHCID 8028—
Product1-benzyl-N,4-dimethylpiperidin-3-amineHCID 994388969%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091208B2
Source datasetuspto-grants-2006_08
ORD IDord-8210397d84ee46a398b1d1f423bf0696
Source noteuspto-grants-2006_08