HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113639Generated: October 29, 2026
Methyl 4-Formylbenzoate → 4-(3,3,3-Trifluoropropenyl)benzoic acid
https://huagongshe.com/reaction/2113639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-Formylbenzoate | HCID 15294 | — |
| Reactant | Diphenyl(2,2,2-trifluoroethyl)phosphine oxide | HCID 11323568 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Product | 4-(3,3,3-Trifluoropropenyl)benzoic acid | HCID 68861492 | 60% |
Reaction Steps
4A Molecular sieves (7 g; activated powder) was suspended in 8.8 ml of 1.0M TBAF in THF and stirred overnight at room temperature under nitrogen. To the solution was added methyl 4-formylbenzoate (160 mg; 0.97 mmol) and 2,2,2-trifluoroethyldiphenylphosphine oxide (415 mg; 1.46 mmol) in 10 ml of anhydrous THF. After stirring overnight, the solvents were evaporated to dryness. The residue was dissolved in EtOAc and washed with water and brine. The organic dried over Na2SO4, filtered and evaporated. The residue was dissolved in 10 ml of THF and 10 ml of 1N NaOH and refluxed for 30 minutes. The mixture was acidified with concentrated HCl and extracted three times with EtOAc. The organic layers were washed with brine and dried over Na2SO4, filtered and evaporated to give the desired product as a brown powder (125 mg; 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432281B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-5f8bf479de784250b30db56d2157228b |
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| Source note | uspto-grants-2008_10 |
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