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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063309Generated: October 31, 2026

Ammonium Acetate → Tert-butyl 4-amino-3,3-dimethylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1063309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-Butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylateHCID 22278899—
SolventMethanolHCID 887—
ProductTert-butyl 4-amino-3,3-dimethylpiperidine-1-carboxylateHCID 10171391—

Reaction Conditions

Temperature25 °C

Reaction Steps

Ammonium acetate (700 g, 9.09 mol) was added to a stirred solution of 1-t-butyloxy carbonyl-3,3-dimethyl-4-piperidone (352 g, 1.55 mol) in methanol (1.0 L). The suspension was stirred for 3 hr at 20-30° C. The reaction mixture was cooled to 0° C. and sodiumcyanoborohydride (45 g, 0.71 mol) was added portion wise over 30 minutes. Cooling was removed and the suspension was stirred for 12 hr at 20-30° C. The reaction mixture was concentrated to dryness, stirred with water (2.0 L) and extracted with 1.0 L×3 dichloromethane. Combined organic extract was washed with water and dried over sodium sulfate. Evaporation of organic solvent afforded the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964966B2
Source datasetuspto-grants-2005_11
ORD IDord-e61591f3213a46df8d6f94577f968336
Source noteuspto-grants-2005_11