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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51860Erstellt: 26. Oktober 2026

p-Xylyl bromide → (4-Methoxy-3-nitro-phenyl)-bis-(4-methyl-benzyl)-amine

https://huagongshe.com/reaction/51860

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Xylyl bromideHCID 7721—
EduktDiisopropylethylamineHCID 81531—
EduktBenzenamine, 4-methoxy-3-nitro-HCID 123071—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(4-Methoxy-3-nitro-phenyl)-bis-(4-methyl-benzyl)-amineHCID 2273697193%

Reaktionsschritte

To a stirred solution of 5.00 g (29.7 mmol) 4-methoxy-3-nitro-phenylamine in 60 ml acetonitrile at 0° C. were added 10.2 ml (59.5 mmol) N-ethyldiisopropylamine and 11.6 g (62.4 mmol) 4-methylbenzyl bromide. Stirring was continued at room temperature for 16 h and then the mixture was diluted with ethyl acetate and washed with 0.5 N hydrochloric acid and then with brine. The organic phase was dried over sodium sulfate and concentrated in vacuo to afford 10.4 g (93%) (4-methoxy-3-nitro-phenyl)-bis-(4-methyl-benzyl)-amine as an orange oil. ES-MS m/e (%): 399 (M+Na+, 18), 377 (M+H+, 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713499B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-ff2ffa8c03f24d1283bb8fd94dc8bf7e
Quellennotizuspto-grants-2004_03