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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1750872Erstellt: 24. Oktober 2026

4-Chloroaniline → N-(4-chlorophenyl)-5-nitronaphthalen-1-amine

https://huagongshe.com/de/reaction/1750872

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChloroanilineHCID 7812—
Edukt1-Bromo-5-nitronaphthaleneHCID 219988—
Edukt1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDimethylacetamideHCID 31374—
ProduktN-(4-chlorophenyl)-5-nitronaphthalen-1-amineHCID 10104323866%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

1-bromo-5-nitronaphthalene (131 mg, 0.52 mmol) was dissolved in DMA (5 mL), and added with 4-chloroaniline (60 mg, 0.47 mmol), Xantphos (27 mg, 0.047 mmol), Pd2(dba)3 (17.2 mg, 0.019 mmol) and CsCO3 (306 mg, 0.94 mmol) at room temperature. The reaction solution was sealed and stirred for about 3 hours under microwave conditions at 140° C. The reaction mixture was cooled to room temperature, diluted with ethyl acetate, and washed with a saturated aqueous solution of sodium bicarbonate and brine. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The concentrated compound purified using silica gel chromatography (ethyl acetate:hexane=1:5 (v/v)) to obtain the title compound (92 mg, 66%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09156852B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-007c4a144d4f44dbac7d13bd595265a8
Quellennotizuspto-grants-2015_10