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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610926Generated: November 3, 2026

Ethyl 5-methoxyindole-2-carboxylate → Ethyl 5-hydroxy-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1610926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-methoxyindole-2-carboxylateHCID 20926—
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-hydroxy-1H-indole-2-carboxylateHCID 9067748.2%

Reaction Steps

Boron tribromide (64.58 g) was added dropwise to a stirred solution of ethyl 5-methoxyindole-2-carboxylate (20 g) in dichloromethane (1000 ml) at −78° C. under an atmosphere of argon. The reaction was allowed to warm to room temperature and stirred for a further 2 hours. The reaction was poured into ice/s aqueous sodium hydrogen carbonate solution with stirring and extracted with ethyl acetate. Combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution, water, aqueous saturated sodium chloride solution and dried. The solution was concentrated in vacuo and the residue was purified by column chromatography using 0-60% diethyl ether, iso-hexane as eluent to yield product as a white solid (9.02 g, 48%). NMR: 1.31 (t, 3H), 4.29 (q, 2H), 6.79 (dd, 1H), 6.90 (dd, 1H), 7.22 (d, 1H), 8.84 (s, 1H), 11.52 (brs, 1H; m/z 206 M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984657B1
Source datasetuspto-grants-2006_01
ORD IDord-75c1cea0c94449f9b990b1a088825811
Source noteuspto-grants-2006_01