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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646942Generated: November 1, 2026

4-Toluenesulfonyl chloride → 1-Tosyl-1H-indole-4-carbaldehyde

https://huagongshe.com/reaction/1646942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
ReactantTetrabutylammoniumHCID 16028—
ReactantIndole-4-carboxaldehydeHCID 333703—
SolventBenzeneHCID 241—
Product1-Tosyl-1H-indole-4-carbaldehydeHCID 1311509358.1%

Reaction Steps

150 ml of 50% sodium hydroxide, 4.75 g of tetrabutylammonium hydrogenosulfate and 30.24 g of p-toluene sulfonyl chloride were added to a suspension of 20 g of indole 4carboxaldehyde in 600 m1 of benzene and the mixture was stirred or 90 minutes at ambient temperature. After decanting and extracting with benzene, the extracts were washed with water, dried and evaporated to dryness under reduced pressure. The 42.1 g of residue were dissolved in 210 ml of benzene at reflux, and the solution was allowed to cool to ambient temperature over 16 hours, then separated to obtain 23.96 g of the desired product melting at 144 to 146° C. The product was used as is for the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05182282
Source datasetuspto-grants-1993_01
ORD IDord-deb4cfc759874f8fbdb7d8ff87c443c5
Source noteuspto-grants-1993_01