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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737062Generated: October 30, 2026

3-(propan-2-yl)-1H-indole → HCID 58975178, compound

https://huagongshe.com/reaction/737062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(propan-2-yl)-1H-indoleHCID 12534824—
ReactantWater ethylacetateHCID 22728543—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chlorideHCID 58975125—
SolventDimethylformamideHCID 6228—
ProductHCID 58975178HCID 58975178—

Reaction Steps

Stir a mixture of 3-isopropyl indole in dry DMF (20 ml) under N2 add potassium t-butoxide 1.0 M (1.2 ml, 1.2 mmol) dropwise. Stir the resulting solution for 30 minutes at ambient temperature. Add 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (0.360 g, 1.1 mmol) portionwise and stir the resulting mixture overnight. Pour the reaction mixture into a mixture of EtOAc—H2O. Separate the EtOAc layer, extract with H2O wash with brine and dry (MgSO4). Filter and evaporate to give the crude product. Chromatograph on the ISCO eluting with hexane-EtOAc to give a white solid (0.150 g). Mass spectrum (m/e) (M+H) 451.1492; found 451.1488.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595339B2
Source datasetuspto-grants-2009_09
ORD IDord-6e6db808672844b2aa9b6035559abfb4
Source noteuspto-grants-2009_09