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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1059729Erstellt: 27. Oktober 2026

Allyl bromide → 3-Allyloxycarbonyl-5-nitrobenzoic acid

https://huagongshe.com/reaction/1059729

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
PatentnummerUS06521612B2
Quelldatensatzuspto-grants-2003_02
ORD IDord-a9325c233d964cd0a6b5dc8d52a6b759
Quellennotizuspto-grants-2003_02