Methanol → Methyl 3-methyl-2-benzofurancarboxylate

HRID 2221441

Reaktionsgleichung

Reaktionsgleichung von HRID 2221441
[CH3:1][C:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:11]([OH:13])=[O:12].[C:14](Cl)(=O)C(Cl)=O.CO>CN(C=O)C.C1COCC1>[CH3:1][C:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:11]([O:13][CH3:14])=[O:12]

Komponenten

6

Versuchsvorschrift

To a solution of 3-methyl-benzofuran-2-carboxylic acid (0.98 g, 5.6 mmol) and catalytic amount of DMF (5 drops) in THF (25 ml) was added oxalyl chloride (0.53 ml, 6.1 mmol). After stirring the solution for 1 h at room temperature, methanol (20 ml) and TEA (7.0 ml) were added. The reaction mixture was stirred overnight at room temperature, then concentrated and dissolved in ethyl acetate (100 ml) and washed with aqueous sodium bicarbonate solution (100 ml). The organic layer was dried over sodium sulfate and concentrated to provide crude methyl 3-methylbenzofuran-2-carboxylate (1.0 g, 5.3 mmol) as a tan solid, which was used without further purification.

Aufarbeitung

  1. stirringThe reaction mixture was stirred overnight at room temperature
  2. concentrationconcentrated
  3. dissolutiondissolved in ethyl acetate (100 ml)
  4. washwashed with aqueous sodium bicarbonate solution (100 ml)
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-c6b527b2c1074afab8ad5326b4ecda9b
Quelldatensatz
uspto-grants-2008_05
Patentnummer
US07368572B2

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