HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507929Generated: November 2, 2026
4-Nitrobenzaldehyde → HCID 5323929, compound
https://huagongshe.com/reaction/507929
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Triethyl 2-fluoro-2-phosphonoacetate | HCID 2734865 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 5323929 | HCID 5323929 | 72% |
Reaction Steps
A solution of ethyl diethylphosphono-2-fluoroacetate (4.90 g, 20.2 mmol) in tetrahydrofuran (40 mL) was stirred under a nitrogen atmosphere at 0° C. and 1.6 M n-butyllithium/hexane solution (13.1 mL, 21.0 mmol) was added dropwise. The reaction mixture was stirred at 0° C. for 30 min, and a solution of 4-nitrobenzaldehyde (3.05 g, 20.2 mmol) in tetrahydrofuran (40 mL) was added dropwise. The mixture was stirred at room temperature for 16 hr, and ice-cooled aqueous ammonium chloride solution was added. The mixture was extracted with ethyl acetate, and the extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (3%-40% ethyl acetate/hexane) to give the title compound (3.46 g, yield 72%) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786165B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-af18e17cc5a84b4fbb7a06219e35158e |
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| Source note | uspto-grants-2010_08 |
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