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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394095Generated: October 26, 2026

Tert-Butylamine → 1-tert-Butyl-4-piperidone

https://huagongshe.com/reaction/394095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Ethyl-1-methyl-4-oxopiperidin-1-ium iodideHCID 11097568—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-tert-Butyl-4-piperidoneHCID 73840—

Reaction Conditions

Temperature78 °C

Reaction Steps

To a solution of 137 mL (1.3 moles) of tert-butylamine in 700 mL of toluene was added solution of 70 g (0.260 moles) of 1-ethyl-1-methyl-4-oxopiperidinium iodide and 2.18 g (0.026 moles) of NaHCO3 in 100 mL of water. The mixture was stirred at 78° C. for 6 h. After it had cooled to rt, the layers were separated and the aq layer was washed with three 200 mL portions of ethyl acetate. The combined organic layers were washed with brine, dried (MgSO4), and concentrated to an oil that purified by distillation under reduced pressure. Fractions distilling at 72° C. at 3 mm were collected to afford the title compound as a colorless liquid. 1H NM(CDCl3, 500 MHz): δ 1.15 (s, 9H), 2.45 (t, 4H, J=6.1 Hz), 2.86 (t, 4H, J=6.1H); Mass spectrum (ESI) 156 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809199B2
Source datasetuspto-grants-2004_10
ORD IDord-375eb11d20fd412ca3859f1fc127a98e
Source noteuspto-grants-2004_10