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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193294Generated: October 30, 2026

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

https://huagongshe.com/reaction/1193294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Producttert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylateHCID 1033329878%

Reaction Steps

A solution of tert-butyl 4-oxopiperidine-1-carboxylate (10.0 g, 50.25 mmol, 1 eq) in THF (50 ml) was slowly added dropwise to an ice-cold (0° C.) suspension of NaH (1.56 g, 65.32 mmol, 1.3 eq) in THF (50 ml), and stirring was carried out for 30 min. Triethyl phosphonoacetate (12.96 ml, 65.32 mmol, 1.3 eq), dissolved in THF (50 ml), was added and stirring was carried out for 2 h at RT. The reaction mixture was hydrolyzed with water (5 ml) and concentrated. The residue was taken up in water (150 ml) and extracted with ethyl acetate (2×300 ml). The combined organic phases were washed with sat. NaCl solution (200 ml), dried over sodium sulfate and concentrated under reduced pressure. After purification by column chromatography (silica gel, 3% ethyl acetate in hexane), the desired product was obtained in the form of a white solid. Yield: 78% (10.5 g, 39.03 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-0334e856f81245799ce721ab7c14a794
Source noteuspto-grants-2014_03