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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 1H-indole-3-acetate | HCID 13067 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl (2-bromo-1H-indol-3-yl)acetate | HCID 53994886 | 50.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410562B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-7aa27b926a1d4a05b2d9e576a7f2d465 |
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| Source note | uspto-grants-2002_06 |
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