Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264627Generated: October 31, 2026

Sodium Chloride → 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carbaldehyde

https://huagongshe.com/reaction/2264627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTriethylamineHCID 8471—
Reactant{1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}methanolHCID 67044165—
Solvent1,2-DichloroethaneHCID 11—
SolventDimethyl SulfoxideHCID 679—
Product1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carbaldehydeHCID 4421080798.4%

Reaction Steps

To a solution of 0.93 g of {1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}methanol and 1.1 mL of triethylamine in 10 mL of 1,2-dichloroethane, a solution of 1.21 g of sulfur trioxide-pyridine complex in 5 mL of DMSO was added under ice cooling, and the resulting mixture was stirred under ice cooling for 1 hour. The solution was poured into a mixed solution of 25 ml of ice water and 25 mL of saturated aqueous sodium chloride solution, the resulting mixture was extracted with 100 mL of ethyl acetate, the extract was washed with 5% aqueous potassium hydrogen sulfate solution, water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with hexane to obtain 0.91 g of 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carbaldehyde as a beige solid. FAB+: 364, 366

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855225B2
Source datasetuspto-grants-2010_12
ORD IDord-a18ca397aefb404880692ac250803299
Source noteuspto-grants-2010_12