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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429614Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 18355197, compound

https://huagongshe.com/reaction/429614

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium hydrideHCID 24758—
ReactantBenzyl 1H-indole-4-carboxylateHCID 12825939—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18355197HCID 1835519759.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium hydride (133 mg) in tetrahydrofuran (5.0 ml) was added dropwise a solution of benzyl indole-4-carboxylate (580 mg) in tetrahydrofuran (5.0 ml) at 0° C. and the mixture was stirred at 0° C. for 1 hour. 4-Toluenesulfonyl chloride (440 mg) was added to the mixture and the solution was stirred at ambient temperature for 1 hour. The reaction was quenched with 1N hydrochloric acid and then the aqueous solution was extracted with ethyl acetate. Drying, filtering and removal of solvents afforded a crude product. The crude product was purified by column chromatography (eluent; n-hexane:ethyl acetate=15:1) to give benzyl 1-(4-toluenesulfonyl)indole-4-carboxylate (560 mg) as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316482B1
Source datasetuspto-grants-2001_11
ORD IDord-9479b6873ffe4858a9af928dae6340fa
Source noteuspto-grants-2001_11