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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23458Erstellt: 23. Oktober 2026

1-Bromo-4-tert-butyl-2-nitrobenzene → 3-tert-Butylaniline

https://huagongshe.com/de/reaction/23458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-4-tert-butyl-2-nitrobenzeneHCID 11253906—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt3-tert-ButylanilineHCID 79334—

Reaktionsschritte

1-Bromo-4-tert-butyl-2-nitro-benzene (18 g) was reduced as described in General Method 3 using 10% palladium on charcoal (1 g) and MeOH (100 mL) in a hydrogen atmosphere (50 psi). The catalyst was filtered, and the solvents were evaporated. The residue was taken in EtOAc (100 mL) and washed with saturated sodium bicarbonate solution and H2O. The solution was dried and concentrated. The residue was purified by flash chromatography to give 3-tert-butyl-phenylamine. MS (APCI): 150 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852711B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-d7f5f06869914232b71e686a20541302
Quellennotizuspto-grants-2005_02