Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109758Generated: November 1, 2026

1-(Triphenylphosphoranylidene)acetone → 3-Buten-2-one,4-(4-CF3-phenyl)-

https://huagongshe.com/reaction/2109758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Triphenylphosphoranylidene)acetoneHCID 15038—
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
Catalyst1-(Triphenylphosphoranylidene)acetoneHCID 15038—
SolventDichloromethaneHCID 6344—
Product3-Buten-2-one,4-(4-CF3-phenyl)-HCID 570885392%

Reaction Steps

4-(Trifluoromethyl)benzaldehyde (25.0 g, 144 mmol) was taken up in 500 mL of DCM. 1-Triphenylphosphoranylidene-2-propanone (48.0 g, 151 mmol) was added. After 5 hours, an additional 3 g of 1-triphenylphosphoranylidene-2-propanone was added. The mixture was stirred for 10 hours. The solvent was removed under reduced pressure, and the residue was triturated with 500 mL of 5% EtOAc/hexanes. The mixture was filtered, removing a large amount of P(O)Ph3. The residue was taken up in 300 mL of 2.5% EtOAc/hexanes and filtered through a pad of silica. The mixture was concentrated under reduced pressure and the residue was found to be (E)-4-(4-(trifluoromethyl)phenyl)but-3-en-2-one (28.3 g, 92.0% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.68-7.60 (m, 4H), 7.52 (d, J=16.43 Hz, 1H), 6.78 (d, J=16.4 Hz, 1H), 2.41 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514566B2
Source datasetuspto-grants-2009_04
ORD IDord-c27ee58d8f324e8da47629071ba7afc9
Source noteuspto-grants-2009_04