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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749788Generated: November 4, 2026

Indole-3-Carboxaldehyde → HCID 86681986, compound

https://huagongshe.com/reaction/1749788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-CarboxaldehydeHCID 10256—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzenesulfonyl chloride, 2,4-dichloro-HCID 204419—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductHCID 86681986HCID 8668198687.5%

Reaction Steps

A solution of 1H-indole-3-carboxaldehyde (0.290 g, 2.00 mmol) in methylene chloride (4 mL) was added with 2,4-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-(2,4-dichlorophenylsulfonyl)-1H-indole-3-carboxaldehyde (0.620 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-6af79d5063ea4928871296cc6698f3f1
Source noteuspto-grants-2015_10