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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7009Erstellt: 23. Oktober 2026

p-Toluenesulfonic acid → Methyl 3-bromo-2-fluorobenzoate

https://huagongshe.com/de/reaction/7009

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktTrimethyl orthoformateHCID 9005—
Edukt3-Bromo-2-fluorobenzoic acidHCID 2736313—
LösungsmittelMethanolHCID 887—
ProduktMethyl 3-bromo-2-fluorobenzoateHCID 2158450584%

Reaktionsschritte

A solution of 3-bromo-2-fluorobenzoic acid (0.219 g, 1 mmol) in dry methanol (5 ml) under nitrogen was treated with trimethylorthoformate (0.22 ml, 2 mmol) and p-toluenesulfonic acid (catalytic amount), and then heated under reflux. After 16 h, the mixture was evaporated and the residue partitioned between water and Et2O. The organic layer was washed with sat. sodium hydrogen carbonate solution, water, brine, dried (MgSO4) and evaporated to give methyl 3-bromo-2-fluorobenzoate (0.195 g, 0.84 mmol, 84%): 1H NMR (CDCl3) δ 7.90–7.85 (m, 1H), 7.71–7.65 (m, 1H), 7.10 (dt, 1H, J=8.0, 1.0 Hz) and 3.94 (s, 3H): MS (EI) 232 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084168B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-d6c9ebd1225d4262acc61210cf49b56e
Quellennotizuspto-grants-2006_08