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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515727Generated: October 27, 2026

Ethyl 5-methoxyindole-2-carboxylate → Ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate

https://huagongshe.com/reaction/515727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-methoxyindole-2-carboxylateHCID 20926—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
ProductEthyl 4-bromo-5-methoxy-1H-indole-2-carboxylateHCID 11460715100%

Reaction Steps

To a suspension of ethyl 5-methoxy-1H-indole-2-carboxylate (5 g, 22.81 mmol) in acetic acid (100 mL) was added bromine (1.169 mL, 22.81 mmol) slowly at room temperature. The reaction mixture was stirred at room temperature for 2 days. The solid was filtered off, washed with acetic acid and hexanes, and dried to give the title compound as a white solid (6.8 g). LCMS m/z=298.6 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108969B2
Source datasetuspto-grants-2015_08
ORD IDord-44b0e97028664c8189804bdb98e3a482
Source noteuspto-grants-2015_08