Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1771693Erstellt: 26. Oktober 2026

Methyl iodide → Methyl 5-bromo-2-methoxy-3-methylbenzoate

https://huagongshe.com/reaction/1771693

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktCesium carbonateHCID 10796—
EduktPotassium CarbonateHCID 11430—
Edukt5-Bromo-2-hydroxy-3-methylbenzoic acidHCID 2764345—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 5-bromo-2-methoxy-3-methylbenzoateHCID 276434677,8%

Reaktionsbedingungen

Temperatur58 °C

Reaktionsschritte

To a solution of 5-bromo-2-hydroxy-3-methyl-benzoic acid (3 g, 12.9 mmol, 1.0 eq) and K2CO3 (5.38 g, 38.9 mmol, 3.0 eq) in acetone (15 mL) was added MeI (5.53 g, 38.9 mmol, 3.0 eq). The mixture was stirred at 58° C. overnight. TLC indicated that the reaction was not completed. Water was added and the aqueous layer extracted with EtOAc. The organic extract was washed with water and brine, dried (Na2SO4) filtered and evaporated in vacuo. The crude solid obtained was dissolved in DMF (20 mL) and Cs2CO3 (6 g, 18.4 mmol, 1.4 eq) added. To the mixture was added MeI (2 mL, 38.95 mmol, 3 eq). The mixture was stirred for 1 h at room temperature, water was added and the aqueous layer was extracted with EtOAc. The combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo to give the title compound as a white solid (2.6 g, 77%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09249085B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-a137cbb6b8e94faca9e92d005cb5808b
Quellennotizuspto-grants-2016_02