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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054107Generated: October 26, 2026

p-Fluoronitrobenzene → 3-methyl-N-(4-nitrophenyl)pyrid-2-amine

https://huagongshe.com/reaction/2054107

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-3-methylpyridineHCID 15347—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-methyl-N-(4-nitrophenyl)pyrid-2-amineHCID 2310447736.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

0.3 g of 4-fluoronitrobenzene, 0.46 g of 2-amino-3-methylpyridine, and 0.353 g of K2CO3 were added to a solution of 2.5 ml of N-methylpyrrolidinone. The reaction medium was heated at 60° C. for 1 hour and 0.286 g of potassium tert-butoxide was then added. Heating was then continued for 6 hours and, after cooling to room temperature, the reaction medium was then poured into a water and ice mixture. The yellow precipitate formed was filtered off, reslurried in water and then dried over P2O5. 0.18 g of 3-methyl-N-(4-nitrophenyl)pyrid-2-amine (7) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329288B2
Source datasetuspto-grants-2008_02
ORD IDord-1d63e4b2be784c96873ad1d1a9773058
Source noteuspto-grants-2008_02