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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297068Generated: October 31, 2026

Acetic Acid → 1-benzyl-N,4-dimethylpiperidin-3-amine

https://huagongshe.com/reaction/1297068

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 numberUS07250420B2
Source datasetuspto-grants-2007_07
ORD IDord-259dfe2331f54857a1e59f326a9ca9ae
Source noteuspto-grants-2007_07