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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117151Generated: October 29, 2026

N-bromobutanimide → HCID 21081597, compound

https://huagongshe.com/reaction/2117151

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 numberUS07439246B2
Source datasetuspto-grants-2008_10
ORD IDord-476077cc2ff3458796bd2762ba03f378
Source noteuspto-grants-2008_10