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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481761Generated: October 27, 2026

Selectfluor → ethyl 5-bromo-3-fluoro-1-methyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1481761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelectfluorHCID 2724933—
ReactantEthyl 5-bromo-1-methyl-1H-indole-2-carboxylateHCID 11637730—
SolventAcetonitrileHCID 6342—
Productethyl 5-bromo-3-fluoro-1-methyl-1H-indole-2-carboxylateHCID 7128519828%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of ethyl 5-bromo-1-methyl-1H-indole-2-carboxylate (2.93 g, 10.39 mmol) in MeCN (52 mL) was added Selectfluor® (3.87 g, 10.92 mmol, 1.05 eq) at 0° C. in three portions with an interval of 10 min. The reaction was stirred at 0° C. for 30 min before it was allowed to warm to room temperature then stirred for an additional 30 min. The reaction was monitored by TLC analysis. Once the starting material was completely consumed, the reaction was quenched with sat. NaHCO3 and then extracted by CH2Cl2 (4×25 mL). The solvent was removed to give a crude product which was purified by flash column chromatography (0-10% EtOAc in hexanes) to afford the desired product (860 mg, 2.87 mmol) in 28% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409905B2
Source datasetuspto-grants-2016_08
ORD IDord-38007c0f59ba44cc8e04f73d8ac9666c
Source noteuspto-grants-2016_08