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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1263606Erstellt: 25. Oktober 2026

Allyl bromide → 3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl ester

https://huagongshe.com/reaction/1263606

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktPotassium CarbonateHCID 11430—
Edukt3-(N-methyl-hydroxycarbamoyl)-5-nitro-benzoic acid allyl esterHCID 22986101—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl esterHCID 2298610083,3%

Reaktionsschritte

A mixture of (8(a)) (0.60 g), allyl bromide (0.28 g), potassium carbonate (0.59 g) and DMF (20 ml) was stirred for 3 hours at ambient temperature under an argon atmosphere. The dimethyl formamide was then evaporated under reduced pressure and the residue dissolved in ethyl acetate (50 ml) and water (50ml). The organic phase was separated, washed with brine (50 ml), dried over magnesium sulphate and evaporated under reduced pressure to dryness to give 3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl ester (8(b)) as a yellow oil (0.571 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06541491B1
Quelldatensatzuspto-grants-2003_04
ORD IDord-c23a47d36c474d0996dc1485abe2d332
Quellennotizuspto-grants-2003_04