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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157741Generated: October 30, 2026

Triethyl phosphonoacetate → HCID 178471800, compound

https://huagongshe.com/reaction/1157741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-oxocyclohexanecarboxylateHCID 317638—
ReactantAmmonium formateHCID 2723923—
ReactantEthanol sodium ethoxideHCID 23706232—
CatalystHCID 178418390HCID 178418390—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 178471800HCID 178471800—

Reaction Steps

To a solution (600 ml) of ethyl 4-oxocyclohexanecarboxylate (150 g) in ethanol was added sodium hydroxide (38.8 g) with stirring at room temperature. The reaction solution was stirred for 1 hr and ethyl diethylphosphonoacetate (192 ml) was added. To this reaction solution was added dropwise 21% sodium ethoxide/ethanol solution (363 ml) with stirring under ice-cooling over 1 hr. The stirring was continued for 1 hr and acetic acid (126 ml) was added. Then ammonium formate (111 g) and palladium carbon (5%, 15 g) were added and the mixture was stirred at 60° C. for 6 hr with heating. The reaction solution was allowed to return to room temperature and insoluble materials were filtered off through celite. The filtrate was concentrated and the obtained residue was diluted with ethyl acetate. The mixture was washed successively with 2N aqueous hydrochloric acid, water and saturated brine. The organic layer was dried over sodium sulfate and sodium sulfate was filtered off. The filtrate was concentrated to give a crudely purified product (180.4 g) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807701B2
Source datasetuspto-grants-2010_10
ORD IDord-5ce172b7b45740f4830bf7f1241b9726
Source noteuspto-grants-2010_10