Methyl iodide → Methyl 2-(3-bromo-2-methoxyphenyl)acetate

HRID 1773975Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1773975
[CH3:1][O:2][C:3](=[O:13])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([Br:11])[C:6]=1[OH:12].[C:14](=O)([O-])[O-].[K+].[K+].IC>CC#N.CCOC(C)=O.O>[CH3:1][O:2][C:3](=[O:13])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([Br:11])[C:6]=1[O:12][CH3:14]

Komponenten

7

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a solution of (3-bromo-2-hydroxy-phenyl)-acetic acid methyl ester (866 mg, 3.5 mmol, 1 eq.) and potassium carbonate (2.44 g, 17.7 mmol, 5 eq.) in MeCN (9 mL), iodomethane (0.67 mL, 10.6 mmol, 3 eq.) was added. The resulting mixture was stirred at 50° C. for 2 hours. The reaction mixture was diluted with AcOEt and water. The layers were separated and the aq. phase was extracted with AcOEt (2×). The comb. org. layers were dried over MgSO4, filtered, and concentrated in vacuo to give the title compound as an orange oil. The product was used without further purification.

Aufarbeitung

  1. customThe layers were separated
  2. extractionthe aq. phase was extracted with AcOEt (2×)
  3. dry with materiallayers were dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-059b8d3803e1430a89e83f9f1a70f243
Quelldatensatz
uspto-grants-2016_02
Patentnummer
US09255090B2

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