HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631793Generated: October 30, 2026
Trifluoroacetic acid → Ethyl (E)-4,4-difluoropent-2-enoate
https://huagongshe.com/reaction/631793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-Pyridyldiphenylphosphine | HCID 621893 | — |
| Reactant | Ethyl 4,4-difluoro-3-hydroxy-pentanoate | HCID 89825740 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (E)-4,4-difluoropent-2-enoate | HCID 118534660 | — |
Reaction Steps
Ethyl 4,4-difluoro-3-hydroxy-pentanoate (3.39 g, 0.0186 mol) was dissolved in THF (20 ml). Diphenyl-2-pyridylphosphin (7.37 g, 0.028 mol) was added followed after five minutes by di-tertbutylazodicarboxylate (2.83 g, 0.028 mol). The mixture was stirred for one hour at room temperature and left standing overnight. The mixture was acidified with trifluoroacetic acid (2 ml) and stirred for one hour at room temperature. The solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and 4N HCl. The phases were separated, the organic phase was washed with 1M HCl (4×), dried over magnesium sulfate and evaporated to dryness. After distillation at 2 mbar 5.99 g were obtained which still contained some solvent but were used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321724B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-d618082ccc9f4e30af60d03b752022ae |
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| Source note | uspto-grants-2016_04 |
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