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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5405Generated: October 26, 2026

tert-Butyl Dimethylphosphonoacetate → Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/reaction/5405

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl DimethylphosphonoacetateHCID 4564495—
ReactantEthyl 2,3-di-oxo-1-azacyclodecane-10-carboxylateHCID 19930804—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylateHCID 54383214—

Reaction Steps

Potassium hexamethyldisilylamide (40.5 mL of a 0.58M solution in toluene, 23.5 mmol) is added to THF (60 mL), and then cooled to 0° C. t-Butyl dimethylphosphonoacetate (4.6 mL, 23.5 mmol) is added dropwise, and the reaction is warmed to room temperature and stirred for 25 minutes. Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (2.83 g, 11.74 mmol) is added in THF (15 mL), and the reaction is stirred at room temperature for 2.5 hours. The reaction is quenched with saturated ammonium chloride, and then extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244889
Source datasetuspto-grants-1993_09
ORD IDord-9f6126e0435c45d1b9864f1d5abc955e
Source noteuspto-grants-1993_09