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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375984Generated: October 29, 2026

4-Toluenesulfonyl chloride → 5-bromo-1-(4-methylbenzenesulfonyl)-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/375984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant5-Bromoindole-3-carbaldehydeHCID 70137—
ReactantLithium diisopropylamide mono(tetrahydrofuran)HCID 10997623—
SolventTetrahydrofuranHCID 8028—
Product5-bromo-1-(4-methylbenzenesulfonyl)-1H-indole-3-carbaldehydeHCID 10384969248.8%

Reaction Steps

To a solution of 5-bromoindole-3-carboxaldehyde (10 g) in dry tetrahydrofuran (75 ml), cooled to -78° C., was added with 2M lithium diisopropylamide/tetrahydrofuran (22.5 ml). After 30 min., the mixture was treated with a solution of tosyl chloride (9.5 g) in dry tetrahydrofuran (75 ml). The mixture was allowed to warm to room temperature overnight and evaporated. The residue was dissolved in dimethylformamide, filtered, and the filtrate was diluted with water. The precipitate was collected and recrystallized from ethanol to give 42 g (25%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488063
Source datasetuspto-grants-1996_01
ORD IDord-3b2a10145c7b4cdfa7444fb262619b0d
Source noteuspto-grants-1996_01