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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1787102Erstellt: 25. Oktober 2026

Dimethylformamide → 2,2,6,7-Tetramethyl-1-benzofuran-3(2H)-one

https://huagongshe.com/reaction/1787102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktOxalyl chlorideHCID 65578—
Edukt2-(2,3-Dimethylphenoxy)-2-methylpropanoic acidHCID 1532013—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,2,6,7-Tetramethyl-1-benzofuran-3(2H)-oneHCID 2311426671%

Reaktionsschritte

To a solution of 2-(2,3-dimethylphenoxy)-2-methylpropionic acid obtained in Reference Example 36 (21.0 g, 101 mmol) in THF (200 mL) was added DMF (0.1 mL), and then to the mixture was added dropwise oxalyl chloride (10.6 mL, 121 mmol). The reaction solution was warmed to room temperature, stirred for 1 hour, and then concentrated under reduced pressure. The residue was dissolved in dichloromethane (200 mL), to which was added aluminum chloride (32.3 g, 242 mmol) at −70° C. or lower, and then warmed to room temperature over 12 hours. The reaction solution was added to water with ice-cooling and dichloromethane was distilled off under reduced pressure, which was extracted with ethyl acetate. The organic layer was washed with water, a saturated sodium hydrogen carbonate solution, water and a saturated brine, and then was dried over anhydrous sodium sulfate. The residue after distilling off the solvent under reduced pressure was crystallized from hexane to obtain 17.5 g (yield 71%) of the title compound. Melting point: 79-81° C. (methanol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07507841B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-6ce2883d770d4f568bd1cdc173c6f12e
Quellennotizuspto-grants-2009_03