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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347547Generated: October 30, 2026

N-bromobutanimide → HCID 21081597, compound

https://huagongshe.com/reaction/347547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 21081635HCID 21081635—
SolventAcetonitrileHCID 6342—
ProductHCID 21081597HCID 2108159798.4%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173031B2
Source datasetuspto-grants-2007_02
ORD IDord-26748b41a6e74f6192339c0ed3c2fd84
Source noteuspto-grants-2007_02