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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863704Generated: October 25, 2026

Water → 5-Bromo-1-methyl-3-indolylacetic acid

https://huagongshe.com/reaction/863704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-3-indoleacetic acidHCID 96734—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-1-methyl-3-indolylacetic acidHCID 19696407—

Reaction Steps

500 mg of a 60% dispersion of sodium hydride in mineral oil were added to solution of 1 g of 5-bromoindole-3-acetic acid in 50 ml of tetrahydrofuran and the mixture was stirred under a nitrogen atmosphere for 1 hour. Thereafter, 820 mg (5.8 mmol) of methyl iodide were added and the mixture was stirred under a nitrogen atmosphere for 24 hours. Then, 5 ml of water were added and the solvent was removed under reduced pressure. The residue was treated with 2M hydrochloric acid and the precipitate formed was filtered off, washed with n-hexane and dried. The obtained solid was recrystallized from diethyl ether to give 5-bromo-1-methyl-3-indolylacetic acid of melting point 192°-194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721245
Source datasetuspto-grants-1998_02
ORD IDord-e0de98826901459eb967bedd29d140e1
Source noteuspto-grants-1998_02