Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859243Generated: October 26, 2026

Potassium Carbonate → Ethyl 2-(2-fluoroethyl)-5-methoxy-1-oxoindane-2-carboxylate

https://huagongshe.com/reaction/859243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoroethyl bromideHCID 12982—
Reactantethyl 5-methoxy-1-oxo-2,3-dihydro-1H-indene-2-carboxylateHCID 12177975—
SolventDimethylacetamideHCID 31374—
ProductEthyl 2-(2-fluoroethyl)-5-methoxy-1-oxoindane-2-carboxylateHCID 16726730—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of ethyl 5-methoxy-1-oxoindane-2-carboxylate (crude product from the preceding two reactions, ˜190 mmol), K2CO3 (53.8 g, 389 mmol) and KI (64.7 g, 390 mmol) in anhydrous dimethylacetamide (792 mL) was added 1-bromo-2-fluoroethane (18.4 mL, 247 mmol) and the mixture was stirred and heated at 65° C. After 20 hours, analysis of an aliquot by NMR showed the reaction to be complete. After cooling to room temperature, most of the dimethylacetamide was removed by evaporation at reduced pressure. The residue was partitioned between EtOAc and water and the organic phase was washed with water (4 times) and brine and dried over Na2SO4. Filtration and removal of the solvent under reduced pressure gave crude ethyl 2-(2-fluoroethyl)-5-methoxy-1-oxoindane-2-carboxylate which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151196B2
Source datasetuspto-grants-2006_12
ORD IDord-2b2bb60d002a4136a34f1ac72f33e75f
Source noteuspto-grants-2006_12