Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746866Generated: November 2, 2026

Potassium Hydroxide → 1-Benzyl-4-methylamino-3,3-dimethylpiperidine

https://huagongshe.com/reaction/746866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant1-Benzyl-3,3-dimethylpiperidin-4-oneHCID 9794413—
SolventMethanolHCID 887—
Product1-Benzyl-4-methylamino-3,3-dimethylpiperidineHCID 22278888—

Reaction Steps

Potassium hydroxide (12.85 g, 230 mmol) was added to the stirred solution of methylamine hydrochloride (15.5 g, 230.0 mmol) in methanol (100 ml) and stirring was continued for 30 min at 30° C. 1-Benzyl-3,3-dimethyl-4-piperidone (5 g, 23.0 mmol), was added to the resulting mixture and stirred for 6 hr. Sodium cyanoborohydride (1.45 g, 23.0 mmol) was added to it and reaction mixture was stirred for 15 hr. The reaction mixture was concentrated to dryness, triturated with water, extracted with chloroform, dried (Na2SO4) and concentrated to give 1-benzyl-4-methylamino-3,3-dimethylpiperidine. Yield 5.3 g (99%), C15H24N2, m/z 233 (M+1), PMR (CDCl3): 0.9 (s, 3H), 1.0 (s, 3H), 1.38 (m, 2H), 1.54 (bs, 1H, D2O exchangeable), 1.68-2.1 (m, 4H), 2.4 (s, 3H), 2.86 (m, 1H), 3.4 (dd, 2H), 7.3 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393957B2
Source datasetuspto-grants-2008_07
ORD IDord-c50f0bc546664eeea362f2ccc96f2f39
Source noteuspto-grants-2008_07