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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786453Generated: October 26, 2026

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

https://huagongshe.com/reaction/1786453

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

A 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 into 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, brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash chromatography on silica gel with n-hexane:ethyl acetate (2:1 v/v) as eluant to afford 5.7 g (72%) of the product as a light-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507736B2
Source datasetuspto-grants-2009_03
ORD IDord-4dd177b61f4645da8471e1b54c07186b
Source noteuspto-grants-2009_03