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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855181Generated: October 26, 2026

Hydrochloric Acid → 5-Bromo-1H-indole-7-carboxylic acid

https://huagongshe.com/reaction/855181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantmethyl 5-bromo-1H-indole-7-carboxylateHCID 24728848—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
Product5-Bromo-1H-indole-7-carboxylic acidHCID 53399257—

Reaction Conditions

Temperature40 °C

Reaction Steps

409 mg of 5-bromo-1H-indole-7-carboxylic acid methyl ester (1.61 mmol) were suspended in a mixture of 1.6 ml 2N NaOH and 1.6 ml ethanol and stirred at 40° C. for 2 h. After cooling down, the mixture was treated with 2N aqueous HCl, and extracted twice with EtOAc. The organic phase was the washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo, leading to 353 mg of 5-bromo-1H-indole-7-carboxylic acid as a light brown solid (85%). MS (ISP) 237.9 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-4e2f62583114470e8c88e093fe7f8b69
Source noteuspto-grants-2007_08