Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21978Generated: October 26, 2026

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

https://huagongshe.com/reaction/21978

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 warned 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 numberUS05426103
Source datasetuspto-grants-1995_06
ORD IDord-abd37e9569de41e18c1a8ba201ccfeea
Source noteuspto-grants-1995_06