Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067985Generated: October 30, 2026

Chlorotrimethylsilane → Ethyl 3-(2-fluoro-5-iodophenyl)-3-oxopropanoate

https://huagongshe.com/reaction/1067985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Fluoro-5-iodobenzoic acidHCID 2778925—
ReactantPotassium ethyl malonateHCID 3446434—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(2-fluoro-5-iodophenyl)-3-oxopropanoateHCID 2239721475.4%

Reaction Steps

To a stirred solution of 5.32 g of 2-fluoro-5-iodobenzoic acid from Preparation No. 28 in 20 mL of THF, under argon, is added 3.9 g of carbonyldiimidazole. In a separate flask, 2.8 mL of chlorotrimethylsilane is added to a mixture of 3.74 g of potassium ethyl malonate in 20 mL of acetonitrile. The mixture is stirred under argon for 18 h, then cooled to 0° C. for the dropwise addition of 6.6 mL of DBU. The mixture is stirred for 3 h at 0° C., then the solution of acyl imidazolide prepared above is added via cannula. After 2 h, the mixture is partitioned between ether and excess dilute HCl, and the organic phase is washed with dilute HCl and brine and dried (MgSO4). Removal of the solvent under reduced pressure left a colorless oil, which is flash chromatographed on silica using 10% ethyl acetate in hexane to provide 5.07 g of the title compound as dense pinkish prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248739B1
Source datasetuspto-grants-2001_06
ORD IDord-e294f4fbfa9e4ac6b5f303e0542a3dcb
Source noteuspto-grants-2001_06