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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2221441Erstellt: 26. Oktober 2026

Methanol → Methyl 3-methyl-2-benzofurancarboxylate

https://huagongshe.com/reaction/2221441

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktOxalyl chlorideHCID 65578—
Edukt3-Methyl-1-benzofuran-2-carboxylic acidHCID 600591—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 3-methyl-2-benzofurancarboxylateHCID 7495394,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07368572B2
Quelldatensatzuspto-grants-2008_05
ORD IDord-c6b527b2c1074afab8ad5326b4ecda9b
Quellennotizuspto-grants-2008_05