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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383213Generated: October 28, 2026

2-Aminobiphenyl → HCID 12545264, compound

https://huagongshe.com/reaction/383213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobiphenylHCID 7015—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantPotassium FluorideHCID 522689—
ProductHCID 12545264HCID 1254526491.1%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 1-fluoro-2-nitrobenzene (13.06 g, 92.6 mmol), 2-aminobiphenyl (31.3 g, 185.2 mmol), and potassium fluoride (8.1 g, 138.9 mmol) was prepared in a 100 mL round bottom flask. The flask was evacuated and replaced with nitrogen. The mixture was heated to 200° C. overnight. The reaction mixture was cooled and ethyl acetate and water were added. The layers were separated and the aqueous layer was extracted with ethyl acetate. The organic layers were dried over magnesium sulfate, filtered, and evaporated. The residue was preabsorbed onto Celite and purified by column chromatography eluting with 0, 2, and 5% ethyl acetate/hexanes. 24.5 g (91%) of product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367223B2
Source datasetuspto-grants-2013_02
ORD IDord-8b5b36b35f764088929926de479edb52
Source noteuspto-grants-2013_02