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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant(2R)-pent-4-en-2-olHCID 6999724—
Reactant2,4-Difluoro-6-hydroxybenzaldehydeHCID 22507919—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(S)-2,4-difluoro-6-(pent-4-en-2-yloxy)benzaldehydeHCID 11830703623.72%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273067B2
Source datasetuspto-grants-2016_03
ORD IDord-744f097f0be748be96735efb2daa2075
Source noteuspto-grants-2016_03