Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512752Generated: November 1, 2026

1-Bromo-4-fluorobenzene → 1-Bromo-4-fluoro-2-nitrobenzene

https://huagongshe.com/reaction/1512752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantPotassium NitrateHCID 24434—
SolventSulfuric AcidHCID 1118—
Product1-Bromo-4-fluoro-2-nitrobenzeneHCID 277338382.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Bromo-4-fluorobenzene (50.0 g) was added to concentrated sulfuric acid (200 mL) slowly at 0° C., followed by slow addition of KNO3 (43.3 g). The resulting mixture was stirred at 0° C. for 1 hour. TLC indicated the reaction was complete. The reaction mixture was poured onto ice slowly, and extracted with EtOAc (3×200 mL). The organic solution was dried over anhydrous sodium sulfate. The dried solution was concentrated to afford 1-bromo-4-fluoro-2-nitrobenzene (D39) (52.0 g) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217028B2
Source datasetuspto-grants-2012_07
ORD IDord-52761997b7bc49148eb090b31612950d
Source noteuspto-grants-2012_07