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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 341879Erstellt: 24. Oktober 2026

Allyl bromide → 3-Allyloxycarbonyl-5-nitrobenzoic acid

https://huagongshe.com/de/reaction/341879

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
Edukt5-Nitroisophthalic acidHCID 12069—
Produkt3-Allyloxycarbonyl-5-nitrobenzoic acidHCID 20655860—

Reaktionsschritte

5-Nitroisophthalic acid (5 g) was converted to the mono allyl ester using one equivalent of allyl bromide (2 ml) using a similar method to that described in example 1. The required acid (2.7 g) was extracted from the organic phase with aqueous NaHCO3. The organic layer contained the di-allyl ester (2.7 g). The mono acid, 3-allyloxycarbonyl-5-nitrobenzoic acid, was obtained as a white solid. Nmr (CDCl3): 4.87 (d, 2H); 5.3-5.5 (q, 2H); 5.97-6.15 (m, 1H); 9.01 (t, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05856321
Quelldatensatzuspto-grants-1999_01
ORD IDord-3b9c539fa1f84be68a147038c98010bb
Quellennotizuspto-grants-1999_01