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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583601Generated: October 25, 2026

Water → 1-Benzyl-5-Bromo-1H-Indole

https://huagongshe.com/reaction/583601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium HydroxideHCID 14797—
Reactant5-BromoindoleHCID 24905—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-5-Bromo-1H-IndoleHCID 28575680%

Reaction Conditions

Temperature30 °C

Reaction Steps

In a suspension of 26.6 g of KOH in 200 ml of dimethylformamide, 20.1 g of solid 5-bromoindole was incorporated while being stirred. The mixture was stirred for 50 minutes at room temperature, and 25.4 g of benzyl chloride was dropwise added to the mixture over a period of 16 minutes at a temperature of not higher than 30° C. The reaction mixture was maintained at 30° C. in an oil bath for 5 hours with stirring. After completion of the reaction, 200 ml of water was added and the thus-formed aqueous phase was extracted with 120 ml of ether three times. The thus-obtained organic phase was washed with water and dried over sodium sulfate overnight. The dried product was concentrated to dryness and then recrystallized from isopropyl ether to give 23.5 g of N-benzyl-5-bromoindole. The yield was 80% by mole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929281
Source datasetuspto-grants-1999_07
ORD IDord-7b241651f8db4175b431fd2f7a415335
Source noteuspto-grants-1999_07