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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384061Generated: October 30, 2026

Triethyl phosphonoacetate → tert-Butyl 3-(2-ethoxy-2-oxoethylidene)azetidine-1-carboxylate

https://huagongshe.com/reaction/384061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-(2-ethoxy-2-oxoethylidene)azetidine-1-carboxylateHCID 4419553062%

Reaction Steps

To an ice-cold solution of ethyl 2-diethoxyphosphorylacetate (25.9 g, 116 mmol) in THF (200 mL) was added carefully NaH (60% dispersion in mineral oil, 4.62 g, 116 mmol) over 25 min. The cold bath was removed and after 30 min, tert-butyl 3-oxoazetidine-1-carboxylate (9.88 g, 57.7 mmol) in THF (40 mL) was added over 5 min. After 30 min, the reaction mixture was quenched with water and extracted twice with ethyl acetate. The combined organics were washed with brine, dried (MgSO4), filtered and concentrated. Purification by column chromatography (6/1 Pet ether/ethyl acetate) gave the ester (8.59 g, 62%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367697B2
Source datasetuspto-grants-2013_02
ORD IDord-0c648d51ec364da0a3a1495bd76370fc
Source noteuspto-grants-2013_02