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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64309Generated: October 27, 2026

Triethyl phosphonoacetate → Ethyl 2-(1-benzylpiperidin-4-ylidene)acetate

https://huagongshe.com/reaction/64309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(1-benzylpiperidin-4-ylidene)acetateHCID 1037786687.5%

Reaction Steps

To a suspension of NaH (318 mg, 7.94 mmol) in THF (20 mL) was added a solution of ethyl 2-(diethoxyphosphoryl)acetate (1.78 g, 7.94 mmol) in THF (5 mL) dropwise over 30 min at 0° C. After stirring for 10 min, a solution of 1-benzylpiperidin-4-one (1.0 g, 5.29 mmol) in THF (5 mL) was added dropwise at 0° C. over 20 min. The mixture was allowed to stir for 60 min. Then, the reaction was quenched with water (10 mL). The mixture was extracted with EA (10 mL×3). The combined organic layers were dried over Na2SO4, concentrated and purified by chromatography column on silica gel using 25% of EA in PE as eluant to give the product (1.2 g, 87.3%) as a yellow oil. MS (ESI, m/e) [M+1]+ 260.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447106B2
Source datasetuspto-grants-2016_09
ORD IDord-7d7b722ee7d9436dbe3caa36e37603e1
Source noteuspto-grants-2016_09