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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226306Generated: October 30, 2026

Triethyl phosphonoacetate → HCID 86603615, compound

https://huagongshe.com/reaction/226306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
ReactantWater ethylacetateHCID 22728543—
ReactantHCID 86095763HCID 86095763—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86603615HCID 8660361575.2%

Reaction Conditions

Temperature15 °C

Reaction Steps

A solution of diethylphosphonoacetic acid ethyl ester (274 mg) in THF (10 ml) was added dropwise to a mixture of 60% sodium hydride in oil (55 mg) in THF (10 mL) with stirring at 10-20° C. under atmospheric pressure of nitrogen, and the reaction mixture was stirred at ambient temperature for 30 minutes. A solution of 6-{[1-(4-chlorobenzoyl)-4-piperidyl]amino}nicotinaldehyde (210 mg) in THF (10 ml) solution was added to the above mixture and resultant mixture was stirred at ambient temperature for 1.5 hour. The reaction mixture was poured into a mixture of AcOEt-H2O and the organic layer was washed with brine and dried over MgSO4. The solvent was evaporated in vacuo and the residue was chromatographed on silicagel eluting with AcOEt-MeOH (95:5). The eluted fractions containing the desired product were collected and evaporated in vacuo to give ethyl (2E)-3-(6-{[1-(4-chlorobenzoyl)-4-piperidyl]amino}-3-pyridyl)acrylate (190 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-a15cbaba40c04c1ab2017bfdd9e25bf1
Source noteuspto-grants-2009_07