HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493503Generated: October 31, 2026
Potassium Carbonate → HCID 86744826, compound
https://huagongshe.com/reaction/1493503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Phenoxybenzyl chloride | HCID 93291 | — |
| Reactant | HCID 15678649 | HCID 15678649 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86744826 | HCID 86744826 | 74.6% |
Reaction Steps
A mixture of 2-[(2,6-dichlorophenyl)amino]-5-hydroxy benzene acetic acid methyl ester (2.5 g, 7.67 mmol) of Example 2F, powdered anhydrous potassium carbonate (0.55 g, 4 mmol), tetrabutylammonium iodide (0.050 g) and dry acetonitrile (50 mL) is stirred at room temperature under nitrogen for 30 min. To the slurry is then added 3-phenoxybenzylchloride (2 g, 9.17 mmol) and the mixture is placed in an oil bath maintained at 65°-70° C. overnight. The solvent is removed and the residue partitioned between water and ethyl acetate (50 mL each). The organic phase is washed with brine and dried (Na2SO4). The solvent is evaporated and the residue (brown oil, 4.2 g) is purified by flash chromatography (on silica Merck 60, hexane-ethyl acetate 85:15) to give the title product (yellow oil, 2.83 g, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05021576 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-c273184d4c93491895d68d38db3b16af |
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| Source note | uspto-grants-1991_06 |
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