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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406968Generated: November 3, 2026

4-Bromo-1-fluoro-2-nitrobenzene → HCID 68054129, compound

https://huagongshe.com/reaction/406968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
Reactanttert-butyl N-(3-aminophenyl)carbamateHCID 12877220—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 68054129HCID 6805412991%

Reaction Steps

A mixture of 4-bromo-1-fluoro-2-nitrobenzene (6.0 g, 27 mmol, Aldrich, Cat. No. 539112) and tert-butyl (3-aminophenyl)carbamate (6.7 g, 32 mmol, Aldrich, Cat. No. 53175) in N-methylpyrrolidinone (30 mL) was heated at 150° C. overnight. The solution was cooled to room temperature (r.t.) and quenched with NaHCO3 aqueous solution, then extracted with ethyl acetate twice. The combined organic phases were washed with brine, and dried over MgSO4. After filtration, the filtrate was concentrated under reduced pressure to afford the desired compound (10.1 g, 91%). LCMS (M+H)+: m/z=408.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754114B2
Source datasetuspto-grants-2014_06
ORD IDord-f30dd574f47846eaa8a020224085ba67
Source noteuspto-grants-2014_06