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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393557Generated: October 27, 2026

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

https://huagongshe.com/reaction/1393557

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 numberUS07345075B2
Source datasetuspto-grants-2008_03
ORD IDord-5bda3df6412f4e94ac057523d2115bfa
Source noteuspto-grants-2008_03