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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582631Generated: November 1, 2026

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

https://huagongshe.com/reaction/1582631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-methoxyindole-2-carboxylateHCID 20926—
ReactantBoron tribromideHCID 25134—
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/saturated 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: δ 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 numberUS06737435B1
Source datasetuspto-grants-2004_05
ORD IDord-9d3f90b361804a7595a9da7dbe982da8
Source noteuspto-grants-2004_05