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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748291Generated: October 26, 2026

Potassium Carbonate → diethyl 1-(2,2-difluoro-3-{[(4-methylphenyl)sulfonyl]oxy}propyl)-1H-indole-2,6-dicarboxylate

https://huagongshe.com/reaction/1748291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,2-Difluoropropane-1,3-diyl bis(4-methylbenzenesulfonate)HCID 44717450—
ReactantDiethyl 1H-indole-2,6-dicarboxylateHCID 44754779—
SolventDimethylformamideHCID 6228—
Productdiethyl 1-(2,2-difluoro-3-{[(4-methylphenyl)sulfonyl]oxy}propyl)-1H-indole-2,6-dicarboxylateHCID 8668239367.8%

Reaction Conditions

Temperature135 °C

Reaction Steps

Diethyl 1H-indole-2,6-dicarboxylate (Intermediate A, 3.5 g, 13.6 mmol), 2,2-difluoropropane-1,3-diyl bis(4-methylbenzenesulfonate) (6.0 g, 14.3 mmol) and K2CO3 (3.9 g, 28.5 mmol) are mixed in DMF (36 mL) and the reaction mixture is separated into 3 fractions. Each fraction is heated in a microwave reactor at 135° C. for 1 h. The 3 fractions are combined, and water (300 mL) and EtOAc (300 mL) are added. The aqueous layer is separated and extracted with EtOAc (3×100 mL). The organic layers are combined, washed with water (3×200 mL), dried (Na2SO4) and concentrated. The crude compound is purified by flash column chromatography using EtOAc in heptane to afford the title compound (4.7 g, 59% pure, 38% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150577B2
Source datasetuspto-grants-2015_10
ORD IDord-4e883693580c4a3ab01b6d54230cdcca
Source noteuspto-grants-2015_10