Methyl iodide → 5-Chloro-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester

HRID 29384Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 29384
[CH2:1]([O:3][C:4]([C:6]1[O:7][C:8]2[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]([OH:17])[C:9]=2[C:10]=1[CH3:11])=[O:5])[CH3:2].IC.[C:20]([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH2:1]([O:3][C:4]([C:6]1[O:7][C:8]2[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]([O:17][CH3:20])[C:9]=2[C:10]=1[CH3:11])=[O:5])[CH3:2]

Komponenten

5

Versuchsvorschrift

To 5-chloro-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester (120 mg, 0.47 mmol) was added 0.3 mL (4.7 mmol) of iodomethane, 130 mg (2 eq) of K2CO3 and 4 mL of DMF. The mixture was stirred at room temperature overnight. The mixture was washed with brine and extracted with ethyl acetate. The combined organic solution was washed with brine and water. Removal of the solvent in vacuo gavel 19 mg (94% yield) of 5-chloro-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester as a white solid.

Aufarbeitung

  1. washThe mixture was washed with brine
  2. extractionextracted with ethyl acetate
  3. washThe combined organic solution was washed with brine and water

Quellen und Nachweise

ORD-Eintrag
ord-ca8c8c18006a4cc6a15b6364c4e26db5
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07420001B2

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