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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521979Generated: October 30, 2026

4-Toluenesulfonyl chloride → 4-Bromo-1-(4-methylbenzene-1-sulfonyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1521979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-1H-pyrrolo[2,3-b]pyridineHCID 22273643—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-Bromo-1-(4-methylbenzene-1-sulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 37818649—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 4-bromo-1H-pyrrolo[2,3-b]pyridine (15 g, 76 mmol) and p-toluenesulfonyl chloride (21.77 g, 114 mmol) in toluene (200 mL) was added a solution of tetrabutylammonium hydrogen sulfate (2.58 g, 7.61 mmol) in water (10 mL) and the mixture was cooled to 0° C. A solution of sodium hydroxide (9.13 g, 228 mmol) in water (30 mL) was added and the mixture was stirred at room temperature overnight. The mixture was diluted with ethyl acetate and the solution was washed with saturated sodium chloride. The organic layer was dried over sodium sulfate, filtered and concentrated to give the title compound. MS (CI) m/z 352 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073922B2
Source datasetuspto-grants-2015_07
ORD IDord-6353068ca86a44d88a33177f5ae86f6b
Source noteuspto-grants-2015_07