HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271213Generated: October 28, 2026
Potassium Hydroxide → HCID 18407219, compound
https://huagongshe.com/reaction/2271213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 9842567 | HCID 9842567 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18407219 | HCID 18407219 | 92.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06333358B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-658239c1848141e399ab359e5b666f91 |
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| Source note | uspto-grants-2001_12 |
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