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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23414Generated: October 27, 2026

Hydrochloric Acid → 6-Bromo-1-cyanomethyl-1H-indole-3-carboxylic Acid

https://huagongshe.com/reaction/23414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromoacetonitrileHCID 11534—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-1H-indole-3-carboxylic acidHCID 15284837—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-Bromo-1-cyanomethyl-1H-indole-3-carboxylic AcidHCID 2257408268%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Bromo-1H-indole-3-carboxylic acid (0.24 g, 1 mmole) was dissolved in anhydrous dimethylformamide (2 ml) and cooled to 0° C. in a nitrogen atmosphere. With stirring, sodium hydride (60% in oil, 0.088 g, 2.2 mmole) was added all at once and the mixture was stirred at this temperature until no more bubbles evolved (ca. 20-30 minutes). Bromoacetonitrile (0.132 g, 1.1 mmole) was added to the reaction mixture which was then allowed to warm to room temperature over the next hour. The reaction mixture was poured into water, acidified with HCl and a precipitate formed. When dried the product weighed 0.190 g (68% yield) and was sufficiently pure to be used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852726B2
Source datasetuspto-grants-2005_02
ORD IDord-e4124114688942ac9062624f8cc731ac
Source noteuspto-grants-2005_02