Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786149Generated: October 31, 2026

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

https://huagongshe.com/reaction/1786149

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 vacuo 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 numberUS07507727B2
Source datasetuspto-grants-2009_03
ORD IDord-fe48ac5603824a4ea55b70df8080cb50
Source noteuspto-grants-2009_03