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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020915Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 67273214, compound

https://huagongshe.com/reaction/1020915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
Reactant4,5-dimethoxy-1H-indoleHCID 1961613—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67273214HCID 6727321486%

Reaction Steps

To 4,5-dimethoxyindole (241 mg, 1.36 mmol) in 5 mL THF at 0° C. was added 82 mg (2.04 mmol, 1.5 eq) of sodium hydride, followed by benzenesulfonyl chloride (260 μL, 2.04 mmol, 1.5 eq). The reaction was warmed to room temperature over 5 h then quenched with H2O and concentrated. The residue was dissolved in CH2Cl2 and extracted with NaHCO3, H2O, aqueous NaCl, dried (Na2SO4), and concentrated. The product was purified by silica gel column chromatography (7/3 hexanes/EtOAc) to give 369 mg of 1-benzenesulfonyl-4,5-dimethoxy-1H-indole (86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716493B2
Source datasetuspto-grants-2014_05
ORD IDord-b47f0ec2eea14c5a800eb6a89605eeda
Source noteuspto-grants-2014_05