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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-bromo-6-fluoro-1H-indole | HCID 11687145 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 5-bromo-6-fluoro-1H-indole-1-acetate | HCID 86640506 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394969B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-6cdfe8153d384caf93eb044a18277248 |
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| Source note | uspto-grants-2013_03 |
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