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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1243362Erstellt: 25. Oktober 2026

Sulfuric Acid → Methyl 3-bromo-5-nitrobenzoate

https://huagongshe.com/reaction/1243362

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktBromineHCID 24408—
EduktMethyl 3-nitrobenzoateHCID 69260—
KatalysatorSulfuric AcidHCID 1118—
KatalysatorHCID 178418844HCID 178418844—
LösungsmittelMethanolHCID 887—
ProduktMethyl 3-bromo-5-nitrobenzoateHCID 23934172%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of methyl 3-nitrobenzoate (122 g, 674 mmol), silver sulphate (100 g, 320.7 mmol) and concentrated sulfuric acid (750 mL) was stirred mechanically and heated at 90° C. To this mixture was added bromine (37 mL), dropwise, over 2 h. The reaction was stirred another hour, cooled and filtered. The filtrate was mixed with 2 L water and 1 Kg crushed ice. The solid was filtered and dried to afford a mixture of the desired methyl ester and free acid hydrolysis product. The mixture was taken up into methanol (1 L), treated with 10 drops concentrated sulfuric acid and refluxed for 12 h. The reaction mixture was allowed to cool and the crystals that were deposited were collected and dried in a desiccator to afford 126 g (72% yield) of methyl 3-bromo-5-nitrobenzoate (EX-119A): 1H NMR (300 MHz, CDCl3) δ 8.65 (s, 1H), 8.44 (s, 1H), 8.37 (s, 1H), 3.94 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07119094B1
Quelldatensatzuspto-grants-2006_10
ORD IDord-19b2dd6100e14109b7c4f2fb640df9d7
Quellennotizuspto-grants-2006_10