Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838923Generated: November 2, 2026

Triethyl phosphonoacetate → HCID 13952644, compound

https://huagongshe.com/reaction/1838923

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 (El+, 70V) 360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677339B2
Source datasetuspto-grants-2004_01
ORD IDord-0a6c8d0a4002456dac917550604dbe77
Source noteuspto-grants-2004_01