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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744229Generated: October 31, 2026

Triethyl phosphonoacetate → HCID 13952644, compound

https://huagongshe.com/reaction/1744229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
Reactant4-Nitrobenzyl bromideHCID 66011—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13952644HCID 1395264422.1%

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 (2.0 g): δH (CDCl3) 8.13 (2H, d, J 8. δHz), 7.37 (2H, d, J 8. δHz), 4.23–4.06 (6H, m), 3.37–3.20 (3H, m), 1.35 (6H, t, J 7.1 Hz), 1.16 (3H, t, ,) 7.1 Hz): m/z (EI+, 70V) 360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015216B2
Source datasetuspto-grants-2006_03
ORD IDord-02244e2f75964cfb9cd0f6921c78b4b1
Source noteuspto-grants-2006_03