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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991336Generated: November 1, 2026

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

https://huagongshe.com/reaction/991336

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) δ 7.43 (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 numberUS06462092B1
Source datasetuspto-grants-2002_10
ORD IDord-f5dff73aa8d0496e9dd0789c4104afbb
Source noteuspto-grants-2002_10