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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883120Generated: November 2, 2026

Hydrochloric Acid → 6-Hydroxy-1-methyl-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/1883120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 6-methoxy-1-methyl-1H-indole-2-carboxylateHCID 4456126—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product6-Hydroxy-1-methyl-1H-indole-2-carboxylic acidHCID 23510098—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a flask under nitrogen was added 576 mg (2.63 mM) of 6-Methoxy-1-methyl-1H-indole-2-carboxylic acid methyl ester and 30 ml dichloromethane. The mixture was cooled to −60° C. in dry ice acetone bath and 16 ml 1M boron tribromide in dichloromethane (16 mM) was added. After stirring 45 minutes at −60° C. the mixture was allowed to warm to room temperature and stirred for 5 hours. The mixture was poured into 200 ml saturated sodium bicarbonate solution and stirred for 30 minutes. Hydrochloric acid was added till acidic, ethyl acetate was added and the mixture filtered through a celite plug to remove insoluble solids. The ethyl acetate layer was separated and the aqueous was extracted two more time with ethyl acetate. The combined ethyl acetate layers were dried over magnesium sulfate, filtered and stripped to give 6-Hydroxy-1-methyl-1H-indole-2-carboxylic acid (M/S, ES-, 190.2 M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759428B2
Source datasetuspto-grants-2004_07
ORD IDord-4a3ad7d51d2f4ca4858a15f6f2cac79d
Source noteuspto-grants-2004_07