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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016574Generated: October 30, 2026

Sodium Methoxide → HCID 18407193, compound

https://huagongshe.com/reaction/1016574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 18407209HCID 18407209—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18407193HCID 1840719397.9%

Reaction Steps

To a solution of 226 mg of sodium methoxide in 5 ml of tetrahydrofuran was added dropwise a solution of 1.22 g of N-chlorocarbonyl-N-(2-methoxybenzyl)-2-phenoxyaniline in 5 ml of tetrahydrofuran under ice-cooling with stirring, followed by stirring at room temperature for 20 minutes. The reaction mixture was concentrated under reduced pressure, poured into water and extracted with ethyl acetate, and the extract was washed with 5% hydrochloric acid, a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, successively, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate−hexane=1:6) and recrystallized from ethyl acetate to give 1.18 g of N-(2-methoxybenzyl)-N-methoxycarbonyl-2-phenoxyaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476056B2
Source datasetuspto-grants-2002_11
ORD IDord-9961e650c54f4c729723b2bdab24707b
Source noteuspto-grants-2002_11