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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242178Generated: October 27, 2026

2-Aminofluorene → 3-(2-Fluorenylamino)-4-nitrophenol

https://huagongshe.com/reaction/1242178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminofluoreneHCID 1539—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
SolventEthyl AcetateHCID 8857—
Product3-(2-Fluorenylamino)-4-nitrophenolHCID 21938121—

Reaction Conditions

Temperature140 °C

Reaction Steps

2.17 g of 3-fluoro-4-nitrophenol and 5 g of 2-aminofluorene were mixed and stirred for 9 hours at 140° C. The raw mixture was taken up in ethyl acetate and water and washed with 1N aqueous hydrochloric acid. The aqueous phase was extracted with ethyl acetate, and the combined organic phases were washed three times with 2N aqueous hydrochloric acid and once with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was chromatographed on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115645B2
Source datasetuspto-grants-2006_10
ORD IDord-5df6270fbb854658a952a7d34ea157d0
Source noteuspto-grants-2006_10