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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054103Generated: November 1, 2026

p-Fluoronitrobenzene → HCID 23104487, compound

https://huagongshe.com/reaction/2054103

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-3-HydroxypyridineHCID 28114—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 23104487HCID 2310448730.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

0.3 g of 4-fluoronitrobenzene, 0.468 g of 2-amino-3-hydroxypyridine, 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 poured into a water and ice mixture. The aqueous phase was extracted with ethyl acetate. The organic phase was dried over MgSO4 and then evaporated to dryness under vacuum. 0.15 g of 2-[(4-nitrophenyl)amino]pyrid-3-ol (3) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329288B2
Source datasetuspto-grants-2008_02
ORD IDord-16b3d5afe6de433bae9990e3ca72631a
Source noteuspto-grants-2008_02