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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033496Generated: November 2, 2026

Allyl iodide → 5-Bromo-1-(prop-2-en-1-yl)-1H-indole

https://huagongshe.com/reaction/1033496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantSodium HydroxideHCID 14798—
Reactant5-BromoindoleHCID 24905—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product5-Bromo-1-(prop-2-en-1-yl)-1H-indoleHCID 1896568360.6%

Reaction Steps

To a stirred mixture of NaOH (204 mg., 5.1 mmol., 1 eq.) in DMSO (10 mL.) was added 5-bromoindole (1.0 g., 5.1 mmol., 1 eq.). The solution was stirred for three hours upon complete dissolution of the NaOH (approximately 1 h.). To this solution was added allyl iodide (0.466 mL., 5.1 mmol., 1 eq.) via syringe. After 2 h. the mixture was diluted with water and extracted 2×with diethyl ether. The organic extracts were combined, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The product was purified by flash column chromatography on silica gel (4:1 hexanes/acetone) affording 730 mg 1-allyl-5-bromoindole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310901
Source datasetuspto-grants-1994_05
ORD IDord-6e9df98a32a0481eb8280ac8a47b2d36
Source noteuspto-grants-1994_05