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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271213Generated: October 28, 2026

Potassium Hydroxide → HCID 18407219, compound

https://huagongshe.com/reaction/2271213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 9842567HCID 9842567—
SolventMethanolHCID 887—
ProductHCID 18407219HCID 1840721992.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of 23 ml of methanol and 3.6 ml of 2 N aqueous potassium hydroxide solution was added 2.26 g of N-acetyl-N-(2-methoxycarbonylbenzyl)-2-phenoxyaniline synthesized in the same manner as in Example 2, followed by stirring at 60° C. for an hour. The reaction mixture was concentrated under reduced pressure, water was added to the residue, and the mixture was made acidic with 2 N hydrochloric acid and extracted with ethyl acetate. The extract was washed with a saturated aqueous sodium chloride solution 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=1:1) to give 2.01 g of N-acetyl-N-(2-carboxybenzyl)-2-phenoxyaniline as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333358B1
Source datasetuspto-grants-2001_12
ORD IDord-658239c1848141e399ab359e5b666f91
Source noteuspto-grants-2001_12