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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187629Generated: October 30, 2026

Ethyl 1H-indole-3-acetate → Ethyl (2-bromo-1H-indol-3-yl)acetate

https://huagongshe.com/reaction/2187629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1H-indole-3-acetateHCID 13067—
ReactantN-bromobutanimideHCID 67184—
SolventDichloromethaneHCID 6344—
ProductEthyl (2-bromo-1H-indol-3-yl)acetateHCID 5399488650.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 15.0 g (73.8 mmol) of ethyl (indol-3-yl)acetate in 75 ml of anhydrous dichloromethane at 0° C. was added 13.1 g (73.8 mmol) of NBS in small portions. The mixture was stirred at 0° C. for 3 h and then quickly concentrated under reduced pressure (argon was used to normalize the pressure after concentration to avoid decomposition due to the product's instability). Column chromatography with 99:1 toluene/ethanol afforded 10.5 g (50%) of the 2-bromoindole as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410562B1
Source datasetuspto-grants-2002_06
ORD IDord-7aa27b926a1d4a05b2d9e576a7f2d465
Source noteuspto-grants-2002_06