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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993466Generated: October 31, 2026

Methanol → HCID 59134404, compound

https://huagongshe.com/reaction/1993466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 59134423HCID 59134423—
SolventChloroformHCID 6212—
ProductHCID 59134404HCID 5913440464%

Reaction Steps

To a solution of 2,2,7,9-tetramethyl-2H-pyrano[2,3-g]quinoline (3.0 g, 12.5 mmol) in chloroform (30.0 mL), a solution of m-chloroperbenzoic acid (4.76 g, 27.6 mmol) in chloroform (12 mL)-methanol (3 mL) was added dropwise at room temperature, and the resulting mixture was stirred at room temperature for 30 minutes. Upon the completion of the reaction, aqueous sodium thiosulfate solution was added to the reaction solution, and it was extracted. The resulting organic phase was washed with sodium hydrogencarbonate and then with aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. After distilling off the solvent, acetic anhydride (12 mL) was added to the residue, and the resulting mixture was stirred at 150° C. for 1 hour. Upon the completion of the reaction, acetic anhydride was distilled off, the residue was neutralized with aqueous sodium carbonate solution, extracted with chloroform, and the resulting organic phase was washed with aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by medium pressure column chromatography (hexane/ethyl acetate=2/1) and the aimed product was obtained (yield: 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652008B2
Source datasetuspto-grants-2010_01
ORD IDord-2c531f5a0b9943d6b263b4aebba136a6
Source noteuspto-grants-2010_01