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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 730253Erstellt: 24. Oktober 2026

Dimethyl 5-nitroisophthalate → Dimethyl 5-aminoisophthalate

https://huagongshe.com/de/reaction/730253

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl 5-nitroisophthalateHCID 83316—
Edukt4-Mercapto-5-aminoisophthalic acid hydrochlorideHCID 68993396—
ProduktDimethyl 5-aminoisophthalateHCID 66831—

Reaktionsschritte

The AB2 monomer, 4-mercapto-5-aminoisophthalic acid hydrochloride, is synthesized in similar fashion, starting with catalytic hydrogenation of dimethyl 5-nitroisophthalate to form the corresponding amine, dimethyl-5-aminoisophthalate, which is then acetylated to protect the amino group. Dimethyl-5-aminoisophthalate is treated with thiocyanogen bromide (generated in-situ from bromine and ammonium thiocynate), and finally hydrolyzed to provide the desired monomer.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07582719B1
Quelldatensatzuspto-grants-2009_09
ORD IDord-99526760e68845849d3b49efed3e0f55
Quellennotizuspto-grants-2009_09