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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966980Generated: October 30, 2026

Acetone → Tert-butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/966980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
Reactant1-tert-Butyl 4-ethyl 4-(prop-2-en-1-yl)piperidine-1,4-dicarboxylateHCID 16218270—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductTert-butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 1001522888%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1-(1,1-Dimethylethyl) 4-ethyl 4-(2-propenyl)-1,4-piperidinedicarboxylate (Description 40, 20.0 g, 67.2 mmol) was dissolved in methanol (300 mL) and dichloromethane (300 mL) and cooled to −78° C. Oxygen was bubbled through the solution for 10 minutes, then ozone for 75 minutes, to give a persistant blue coloration. Oxygen was bubbled through the solution for 10 minutes, then nitrogen for 10 minutes. Sodium borohydride (5.1 g, 135 mmol) was added and the mixture was stirred at −78° C. for 1 hour. Further sodium borohydride (5.1 g, 135 mmol) was added and the mixture was stirred at room temperature for 16 hours. Acetone (75 mL) was added and the mixture was stirred at room temperature for 10 minutes. Water (50 mL) was added and the organic solvent was evaporated under reduced pressure. Saturated aqueous ammonium chloride (500 mL) was added and the mixture was extracted with ethyl acetate (2×500 mL). The combined organic fractions were washed with aqueous citric acid (10%, 500 mL), saturated aqueous sodium hydrogen carbonate (500 mL) and brine (200 mL), dried (Na2SO4) and the solvent was evaporated under reduced pressure to give the title compound (15.0 g, 88%). 1H NMR (400 MHz, CDCl3) δ 4.31 (2H, t, J 7 Hz), 3.97-3.87 (2H, m), 3.17-3.07 (2H, m), 2.20 (2H, t, J 7 Hz), 1.92-1.82 (2H, m), 1.60-1.45 (2H, m), and 1.45 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953792B2
Source datasetuspto-grants-2005_10
ORD IDord-64bebaaeae754e2e93e02c6236858b4b
Source noteuspto-grants-2005_10