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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120123Generated: November 1, 2026

Triethyl phosphonoacetate → HCID 13952644, compound

https://huagongshe.com/reaction/2120123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
Reactant4-Nitrobenzyl bromideHCID 66011—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13952644HCID 1395264422.2%

Reaction Steps

Ethyl 2-(diethoxyphosphoryl)acetate (5.0 ml, 25.2 mmol) was added to a suspension of sodium hydride (60% in mineral oil, 1.10 g, 27.6 mmol) in THF (40 ml) at 0°. After 30 min at room temperature, a solution of 4-nitrobenzylbromide (5.42 g, 25.2 mmol) in THF (40 ml) was added over 30 min. The reaction mixture was stirred for 2 h at room temperature, quenched with water and partitioned between Et2O and water. The aqueous phase was extracted with Et2O and the combined organic layers washed with brine, dried (MgSO4) and evaporated in vacuo. Column chromatography (silica; MeOH/DCM, 1:49) gave the title compound as a pale yellow oil (2.01 g): δH (CDCl3) 8.13 (2H, d, J 8.8 Hz), 7.37 (2H, d, J 8.8 Hz), 4.23-4.06 (6H, m), 3.37-3.20 (3H, m), 1.35 (6H, t, J 7.1 Hz), 1.16 (3H, t, J 7.1 Hz): m/z (EI+, 70V) 360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689781B2
Source datasetuspto-grants-2004_02
ORD IDord-6e7f018bdbbf428b9c52648b6b32b4d7
Source noteuspto-grants-2004_02