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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376280Generated: October 30, 2026

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

https://huagongshe.com/reaction/2376280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(2,3-Dimethylphenoxy)-2-methylpropanoic acidHCID 1532013—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,2,6,7-Tetramethyl-1-benzofuran-3(2H)-oneHCID 2311426671%

Reaction Steps

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 ethyl acetate-hexane to obtain 17.5 g (yield 71%) of the title compound. Melting point: 79-81° C. (methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465815B2
Source datasetuspto-grants-2008_12
ORD IDord-ef1338d74df44c88a0aafef02ac99e61
Source noteuspto-grants-2008_12