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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1660803Erstellt: 26. Oktober 2026

Benzyl Bromide → Methyl 4-benzyloxy-3-nitrobenzoate

https://huagongshe.com/reaction/1660803

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
EduktBenzoic acid, 4-hydroxy-3-nitro-, methyl esterHCID 66835—
LösungsmittelAcetoneHCID 180—
ProduktMethyl 4-benzyloxy-3-nitrobenzoateHCID 289857—

Reaktionsschritte

A solution of 4-hydroxy-3-nitro-benzoic acid methyl ester (30 g, 152 mmol) in acetone (1000 mL) was charged into a 2 L reactor and treated with K2CO3 (31.5 g, 228 mol) and benzyl bromide (52 g, 36.1 mL, 304 mmol). The mixture was mechanically stirred at heated at reflux for 16 hours under a light argon flux. After cooling to room temperature the solvent was evaporated. The residue was taken up in ethyl acetate/water and the two phases were separated. The aqueous phase was extracted three times with ethyl acetate (total solvent volume: 1.5 L, total water volume 1 L). The combined organic phases were dried over sodium sulfate and evaporated. 4-Benzyloxy-3-nitro-benzoic acid methyl ester thus obtained was used crude in the following reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08030308B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-7cddeaed8130442db8fbd55c3661e0c9
Quellennotizuspto-grants-2011_10