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HRID 2303569Erstellt: 26. Oktober 2026

Methyl 3,5-dinitro-4-(4-methoxyphenoxy)-benzoate → Methyl 3,5-diamino-4-(4-methoxyphenoxy)benzoate

https://huagongshe.com/reaction/2303569

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 3,5-dinitro-4-(4-methoxyphenoxy)-benzoateHCID 9819693—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelAcetic AcidHCID 176—
ProduktMethyl 3,5-diamino-4-(4-methoxyphenoxy)benzoateHCID 994787086%

Reaktionsschritte

To a Parr shaker bottle containing a suspension of methyl 3,5-di-nitro-4-(4-methoxyphenoxy)-benzoate (20.2 g; 77.5 mmol) in glacial acetic acid (80 mL) was added 10% palladium on charcoal (0.7 g). The bottle was shaken under an atmosphere of hydrogen (3 atm) until no more hydrogen was consumed. The catalyst was filtered off and the resulting solution concentrated to approximately 10 mL. The residue was dissolved in acetone (50 mL) and heated on a steam bath while water (100 mL) was added in portions. Upon cooling, medium brown needles formed which were collected by suction filtration and dried to give 7.1 g (86%) of methyl 3,5-diamino-4-(4-methoxyphenoxy)benzoate. 300 MHz 1H NMR (CDCl3) d 3.73 (s, 3H, OCH3), 3.80 (bs, 4H, ArNH2) 3.86 (s, 3H, OCH3), 6.84 (m, 4H, ArH), 6.91 (s, 2H, ArH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06433012B1
Quelldatensatzuspto-grants-2002_08
ORD IDord-7304d826ee9b4a84b296d67dfa8aa628
Quellennotizuspto-grants-2002_08