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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207338Generated: November 1, 2026

Dimethyl Carbonate → 1-tert-Butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/2207338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl CarbonateHCID 12021—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
CatalystMethanolHCID 887—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-tert-Butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylateHCID 1127689381%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 60% sodium hydride (3.5 g, 88 mMol) in dry toluene (50 mL), dimethyl carbonate (4.32 g, 48.0 mMol) was added dropwise in 0.5 h at room temperature under an atmosphere of nitrogen. After addition of a few drops of methanol, a solution of 1-tert-butoxycarbonyl-4-piperidone (4.8 g, 24 mMol) dissolved in dry toluene (20 mL) was added dropwise to the reaction mixture while stirring at 80° C. over 1 h. The reaction mixture was stirred for 3 h at the same temperature and then cooled to 0° C. (ice bath) and adjusted to pH 6-6.5 with acetic acid. The resulting cold mixture was diluted with water (10 mL) and adjusted to pH 8 with 5% sodium hydroxide solution. The toluene layer was separated and the aqueous layer was extracted with toluene (20 mL). The combined organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure The compound was dried in vacuum to give methyl-1-tert-butoxycarbonyl-4-oxo-3-piperidine carboxylate (5.0 g, 80%). The compound obtained was carried to next reaction without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376437B2
Source datasetuspto-grants-2016_06
ORD IDord-c26678e70895483c887b93141eb51258
Source noteuspto-grants-2016_06