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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749785Generated: November 2, 2026

Indole-3-Carboxaldehyde → HCID 86681982, compound

https://huagongshe.com/reaction/1749785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-CarboxaldehydeHCID 10256—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant2,3-Dichlorobenzene-1-sulfonyl chlorideHCID 2734222—
SolventDichloromethaneHCID 6344—
ProductHCID 86681982HCID 8668198280.2%

Reaction Steps

A solution of 1H-indole-3-carboxaldehyde (0.290 g, 2.00 mmol) in methylene chloride (4 mL) was added with 2,3-dichlorophenylsulfonyl chloride (0.589 g, 2.40 mmol) and diisopropylethylamine (0.310 g, 2.40 mmol), and the mixture was stirred overnight at room temperature. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate to terminate the reaction, and then extracted three times with methylene chloride. The organic layer was dried over anhydrous magnesium sulfate, then the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain 1-(2,3-dichlorophenylsulfonyl)-1H-indole-3-carboxaldehyde (0.568 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-68713a52704f49d8b20659cc28b84f2f
Source noteuspto-grants-2015_10