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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063297Generated: November 2, 2026

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

https://huagongshe.com/reaction/1063297

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 223 (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 numberUS06964966B2
Source datasetuspto-grants-2005_11
ORD IDord-08b750a5045d4057ba2ea3aeaa61d49b
Source noteuspto-grants-2005_11