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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166055Generated: October 30, 2026

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

https://huagongshe.com/reaction/1166055

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 dry 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 (MgSO4). The solution was concentrated in vacuo and the residue was purified by column chromatography using 0-60% diethyl ether iso-hexane as eluent to give product as a white solid (9.02 g, 48%); NMR δ(CD3SOCD3) 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 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613760B1
Source datasetuspto-grants-2003_09
ORD IDord-b927751d9faf46ed9523f7ab2659f177
Source noteuspto-grants-2003_09