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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076374Generated: October 31, 2026

Potassium Carbonate → HCID 57603291, compound

https://huagongshe.com/reaction/2076374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoroethyl bromideHCID 12982—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 6-chloro-5-methoxy-1-oxoindane-2-carboxylateHCID 46941894—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventDimethylacetamideHCID 31374—
ProductHCID 57603291HCID 57603291—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of ethyl 6-chloro-5-methoxy-1-oxoindane-2-carboxylate (crude product from the preceding step, ˜141 mmol) in anhydrous dimethylacetamide (540 mL) was added K2CO3 (39 g, 282 mmol), KI (46.8 g, 282 mmol) and 1-bromo-2-fluoroethane (13.5 mL, 183 mmol) and the mixture was stirred and heated at 65° C. for 6 hours. The reaction mixture was diluted with THF (540 mL) and water (540 mL) and then cooled to 0° C. and treated with 5N aqueous NaOH (84 mL, 423 mmol). After 2 hours at 0° C., the reaction was quenched with 1N aqueous HCl (˜450 mL). Most of the THF was removed by rotary evaporation under reduced pressure and the aqueous residue was extracted with EtOAc. The organic layer was washed with saturated NaHCO3, dried over MgSO4, filtered through a pad of silica gel and concentrated to give 6-chloro-2-(2-fluoroethyl)-5-methoxyindan-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923568B2
Source datasetuspto-grants-2011_04
ORD IDord-2e028ae9a6bd469b8d583865fb91d88c
Source noteuspto-grants-2011_04