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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168196Generated: October 30, 2026

Ammonium Acetate → tert-Butyl 4-amino-3-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/2168196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-Butyl 3-methoxy-4-oxopiperidine-1-carboxylateHCID 57363786—
SolventMethanolHCID 887—
Producttert-Butyl 4-amino-3-methoxypiperidine-1-carboxylateHCID 53396191—

Reaction Steps

To a solution of 1,1-dimethylethyl 3-(methyloxy)-4-oxo-1-piperidinecarboxylate D18 (2.9 g) in MeOH (100 ml), was added sodium cyanoborohydride (7.9 g, 126 mmol) and ammonium acetate (9.7 g, 126 mmol) at R.T. The reaction mixture was stirred for 4 hours. The resulting mixture was concentrated in vacuo, dissolved in water, basified with sodium hydroxide to pH10 and extracted with DCM. The organic layer was dried over anhydrous MgSO4, concentrated in vacuo to get the desired product D19 in 2.85 g. LCMS [MH+] [email protected] min (5 min run)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045485B2
Source datasetuspto-grants-2015_06
ORD IDord-39b0db23f22f48d08747b3ea32266c1e
Source noteuspto-grants-2015_06