HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120123Generated: November 1, 2026
Triethyl phosphonoacetate → HCID 13952644, compound
https://huagongshe.com/reaction/2120123
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13952644 | HCID 13952644 | 22.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689781B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-6e7f018bdbbf428b9c52648b6b32b4d7 |
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| Source note | uspto-grants-2004_02 |
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