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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48062Generated: October 27, 2026

1-Diethoxyphosphorylpropan-2-one → 4-[3-(Trifluoromethoxy)phenyl]-3-buten-2-one

https://huagongshe.com/reaction/48062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Diethoxyphosphorylpropan-2-oneHCID 14028—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Trifluoromethoxy)benzaldehydeHCID 605139—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
Product4-[3-(Trifluoromethoxy)phenyl]-3-buten-2-oneHCID 6934411854%

Reaction Steps

Ex-626A) Tetrabutylammonium iodide (0.4 g, 0.05 mol) was added to a well-stirred biphasic mixture of 12 mL of 50% NaOH and 20 mL of methylene chloride under a nitrogen atmosphere. A solution of 3-trifluoromethoxybenzaldehyde (4.0 g, 0.021 mol) and diethyl (2-oxopropyl)phosphonate (4.08 g, 0.021 mol) in 4.0 mL of methylene chloride was added dropwise to the stirred solution. The resulting mixture was stirred at room temperature for 15 min, then quenched with water and extracted with hexane. The hexane layer was dried over MgSO4. The crude product was purified by flash column chromatography on silica gel eluting with 1:10 ethyl acetate in hexane to give 2.6 g (54%) of the desired 4-[3-(trifluoromethoxy)phenyl]-3-buten-2-one product as a yellow oil. 1H NMR (CDCl3) δ7.43 (m, 4H), 7.20 (d, 1H), 6.65 (d, 2H), 2.29 (s, 3H). 19F NMR (CDCl3) δ−62.05 (s, 3F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699898B2
Source datasetuspto-grants-2004_03
ORD IDord-0ae043e1bfba43f78f3d7cfab4c39611
Source noteuspto-grants-2004_03