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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1977350Erstellt: 25. Oktober 2026

Allyl bromide → 3-Allyloxycarbonyl-5-nitrobenzoic acid

https://huagongshe.com/reaction/1977350

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktPotassium CarbonateHCID 11430—
Edukt5-Nitroisophthalic acidHCID 12069—
Edukt4-Acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-carboxypyrrolidineHCID 13504324—
LösungsmittelDimethylacetamideHCID 31374—
Produkt3-Allyloxycarbonyl-5-nitrobenzoic acidHCID 20655860—
Produkt3-amino-5(N-methyl-methoxycarbamoyl)-benzoic acid allyl esterHCID 22986142—

Reaktionsschritte

Starting material (1(c)) was prepared as described in Example 1. Starting material 7(d) was prepared as follows. A mixture of potassium carbonate (17.00 g), 5-nitroisophthalic acid (52.00 g), allyl bromide and dimethylacetamide (400 ml) was stirred at 90° for 4 h. Dimethylacetamide was evaporated away under reduced pressure and the residue was dissolved in ethyl acetate. washed with water (2×300 ml) and then extracted with aqueous saturated sodium bicarbonate solution (3×300 ml). The extracts were combined. acidified to pH 4 with concentrated hydrochloric acid and reextracted with ethyl acetate (2×300 ml). The extracts were combined, washed with water (300 ml), dried over magnesium sulphate and evaporated under reduced pressure to give 5-nitro-isophthalic acid 3-allyl ester (7(a)) as a cream solid (39.48 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06232338B1
Quelldatensatzuspto-grants-2001_05
ORD IDord-5c07b5f909e54b85831969a35cf2c882
Quellennotizuspto-grants-2001_05