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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761175Generated: November 1, 2026

Triethyl phosphonoacetate → tert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate

https://huagongshe.com/reaction/1761175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylateHCID 10333298—

Reaction Steps

To a solution of 9.1 g of 60% oily sodium hydride in 200 ml of tetrahydrofuran, 38.0 ml of ethyl diethylphosphonoacetate was added dropwise under cooling with ice, stirred for 20 minutes, and thereafter a solution of 31.4 g of 1-t-butoxycarbonyl-4-piperidone in 500 ml of tetrahydrofuran was added dropwise, followed by 40 minutes' stirring at the same temperature. The reaction liquid was diluted with ethyl acetate, washed successively with aqueous ammonium chloride solution, water and saturated brine, and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the residue was recrystallized from methanol to provide 33.5 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846835B2
Source datasetuspto-grants-2005_01
ORD IDord-fb7395e65a7248a998c2d29325ae2596
Source noteuspto-grants-2005_01