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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990540Generated: October 31, 2026

Dichloromethane → HCID 70149708, compound

https://huagongshe.com/reaction/990540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-Diethoxyphosphorylpropan-2-oneHCID 14028—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Trifluoromethoxy)benzaldehydeHCID 605139—
CatalystTetrabutylammonium IodideHCID 67553—
ProductHCID 70149708HCID 7014970854%

Reaction Steps

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[-(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 numberUS06458852B1
Source datasetuspto-grants-2002_10
ORD IDord-b485108bf0714e50b08b7c8da93aa274
Source noteuspto-grants-2002_10