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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105446Generated: October 26, 2026

Boron tribromide → 6-Bromo-5-hydroxy-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2105446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 6-Bromo-5-methoxyindole-2-carboxylateHCID 14546582—
SolventDichloromethaneHCID 6344—
Product6-Bromo-5-hydroxy-1H-indole-2-carboxylic acid ethyl esterHCID 6701790772.2%

Reaction Steps

The solution of 8.30 g (27.8 mmol) 6-bromo-5-methoxy-1H-indole-2-carboxylic acid ethyl ester (prepared according to J. Org. Chem. 1974, 39, 3580) in 160 mL dichloromethane was cooled to −78° C. At this temperature, 55.7 mL boron tribromide (55.7 mmol; 1M solution in dichloromethane) were added. The solution was allowed to warm to room temperature and after 30 min. the solution was poured on 10% aqueous sodium bicarbonate solution, the phases were separated and the aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with water followed by brine, dried over magnesium sulfate, filtered and evaporated. The residue was flash-chromatographed on silica gel with n-hexane:ethyl acetate (2:1 v/v) as eluant to give 5.7 g (72%) of the product as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579351B2
Source datasetuspto-grants-2009_08
ORD IDord-6cf72996429d4186985615eefc126f91
Source noteuspto-grants-2009_08