Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431952Generated: November 2, 2026

2,3,4,5-Tetrafluorobenzoyl chloride → Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoate

https://huagongshe.com/reaction/1431952

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
ReactantPotassium ethyl malonateHCID 3446434—
ReactantMagnesium ChlorideHCID 5360315—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—

Reaction Steps

Potassium ethyl malonate (3.66 g, 21.5 mmol), MgCl2 (2.44 g, 25.7 mmol) and TEA (2.05 g, 20.3 mmol) were mixed in acetonitrile (70 ml) at 10-15° C. for 2.5 hr. 2,3,4,5-tetrafluorobenzoyl chloride (2.00 g, 10.3 mmol) in acetonitrile (10 ml) was added at 0° C. over 15 min followed by a second addition of TEA (0.23 g, 2.3 mmol). After allowing to warm to RT, the mixture was stirred for 16 hr. After removal of volatiles in vaccuo Toluene (30 ml) was added and removed in vacuo. Following the addition of toluene (60 ml), HCl 1.5 M (40 ml) was added cautiously, ensuring the temperature did not exceed 25° C. The organic fraction was washed with HCl 1.5 M (2×25 ml) and water (2×25 ml), dried over MgSO4 and reduced to a light orange oil in vacuo ([M+1]+ 265, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612063B2
Source datasetuspto-grants-2009_11
ORD IDord-2465959bad2f43f79221100ebc3c25ae
Source noteuspto-grants-2009_11