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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760949Generated: October 30, 2026

Sodium Acetate → tert-Butyl 4-(methylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1760949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventMethanolHCID 887—
Producttert-Butyl 4-(methylamino)piperidine-1-carboxylateHCID 15380702—

Reaction Conditions

Temperature25 °C

Reaction Steps

Powdered molecular seives (3 Å, 5.2 g), methylamine hydrochloride (16.96 g, 251 mmol), anhydrous sodium acetate (41.21 g, 502 mmol), and 95% sodium cyanoborohydride (3.99 g, 60 mmol) were added sequentially to a solution of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester in methanol (400 mL) at 0° C., and the mixture was allowed to warm to 25° C. over several hours. After 18 hours at 25° C., the reaction mixture was filtered thru Celite®, the solids washed with methanol and ethyl acetate, and the filtrate concentrated. The residue was dissolved in ethyl acetate and the resulting solution washed twice with 2N NaOH, once with brine, dried and concentrated to an oil (12.79 g, 119%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846820B2
Source datasetuspto-grants-2005_01
ORD IDord-92309b3373064234b5d5443f4787b1b9
Source noteuspto-grants-2005_01