HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347547Generated: October 30, 2026
N-bromobutanimide → HCID 21081597, compound
https://huagongshe.com/reaction/347547
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 21081635 | HCID 21081635 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21081597 | HCID 21081597 | 98.4% |
Reaction Steps
To a solution of 4-(2-fluoro-4-nitrophenoxy)-1-((2-(trimethylsilyl)ethoxy) methyl)-1H-pyrrolo[2,3-b]pyridine (2.40 g, 5.96 mmol) in 20 mL of acetonitrile at 0° C. was added a solution of NBS (1.01 g, 5.69 mmol, Aldrich) in 10 mL of acetonitrile. The reaction mixture was stirred at 0° C. for 30 min, quenched by the addition of cold water (50 mL), and extracted with EtOAc (3×120 mL). The combined organic extracts were dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, eluting with dichloromethane) to afford the desired product (2.70 g, 94%) as a light yellow oil. MS(ESI+) m/z 482.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173031B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-26748b41a6e74f6192339c0ed3c2fd84 |
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| Source note | uspto-grants-2007_02 |
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