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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945308Generated: November 1, 2026

Ethyl bromoacetate → Ethyl 5-bromo-6-fluoro-1H-indole-1-acetate

https://huagongshe.com/reaction/1945308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant5-bromo-6-fluoro-1H-indoleHCID 11687145—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-bromo-6-fluoro-1H-indole-1-acetateHCID 86640506—

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (81 mg, 3.21 mmol) was added to a 0° C. solution of 5-bromo-6-fluoro-1H-indole (0.343 g, 1.60 mmol) in THF (16 mL). The reaction mixture was stirred at 0° C. for 15 min, then ethyl bromoacetate (0.535 mL, 4.81 mmol) was added. The reaction was stirred at rt for 1 h, then partitioned between water and EtOAc. The aqueous layer was extracted with EtOAc and the combined organic layers were washed with brine, dried (Na2SO4), filtered, and concentrated. The crude product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394969B2
Source datasetuspto-grants-2013_03
ORD IDord-6cdfe8153d384caf93eb044a18277248
Source noteuspto-grants-2013_03