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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264625Generated: October 31, 2026

p-Bromobenzenesulfonyl chloride → ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate

https://huagongshe.com/reaction/2264625

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
Reactant18-Crown-6HCID 28557—
ReactantEthyl indole-2-carboxylateHCID 73125—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Productethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylateHCID 6704396795.3%

Reaction Steps

To a solution of 0.5 g of potassium t-butoxide and 0.1 g of 18-crown-6 in 3 mL of THF, a mixed solution of 0.7 g of ethyl 1H-indole-2-carboxylate and 3 mL of THF was added, and the resulting mixture was stirred at room temperature for 30 minutes. The solution was cooled with ice, 1.13 g of 4-bromobenzenesulfonyl chloride was added, and the resulting mixture was stirred at room temperature for 5 hours. To the solution was added 60 mL of ethyl acetate, the resulting mixture was washed with water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:5) to obtain 1.44 g of ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate as a pale yellow syrup. FAB+: 408, 410

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855225B2
Source datasetuspto-grants-2010_12
ORD IDord-d6d5cf222d6e411eb1e67403140e4b05
Source noteuspto-grants-2010_12