HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921124Generated: October 25, 2026
Triphenylphosphine → (S)-2,4-difluoro-6-(pent-4-en-2-yloxy)benzaldehyde
https://huagongshe.com/reaction/921124
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | (2R)-pent-4-en-2-ol | HCID 6999724 | — |
| Reactant | 2,4-Difluoro-6-hydroxybenzaldehyde | HCID 22507919 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2,4-difluoro-6-(pent-4-en-2-yloxy)benzaldehyde | HCID 118307036 | 23.72% |
Reaction Steps
To a solution of 2,4-difluoro-6-hydroxybenzaldehyde (1.0 g, 6.33 mmol) in THF (14 ml) were added (R)-(−)-pent-4-en-2-ol (1.090 g, 12.65 mmol) and triphenylphosphine (2.157 g, 8.22 mmol). To this mixture was added dropwise DIAD (1.599 ml, 8.22 mmol) (exotherm) and stirred at rt. After 20 h, the mixture was diluted with Et2O and washed with 1N NaOH followed by water (3×'s) then brine, dried (Na2SO4), filtered and concentrated. The crude was purified by flash chromatography (Biotage; 0%-50% EtOAc/hexane; 10 CV) to give (S)-2,4-difluoro-6-(pent-4-en-2-yloxy)benzaldehyde (0.3394 g, 1.500 mmol, 23.72% yield) as a pale yellow oil. 1H NMR (400 MHz, CDCl3) δ: 10.33 (s, 1H), 6.67-6.32 (m, 2H), 6.04-5.63 (m, 1H), 5.32-5.00 (m, 2H), 4.66-4.40 (m, 1H), 2.68-2.28 (m, 2H), 1.41 (d, J=6.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273067B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-744f097f0be748be96735efb2daa2075 |
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| Source note | uspto-grants-2016_03 |
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