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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899455Generated: October 31, 2026

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

https://huagongshe.com/reaction/1899455

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 numberUS05571923
Source datasetuspto-grants-1996_11
ORD IDord-09ea2a946f3b4ef8a9ec62fd29b8a648
Source noteuspto-grants-1996_11