Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Ethoxyphenol | HCID 12150 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 23716089 | HCID 23716089 | — |
Reaction Steps
In a 50-ml flask at ambient temperature 4-ethoxy-phenol (Aldrich) (1492 mg, 10.8 mmoles) was stirred with 2.0 M aqueous KOH (5.50 ml) to form potassium 4-ethoxyphenolate. Methyl 4-chloro-3,5-dinitrobenzoate (Ullmann, 1909, Annalen der Chemie 366:92-93; commercial source: Spectrum Chemical Company, Gardena, Calif.; 2606 mg, 10.0 mmoles) was added, the mixture heated to reflux for 1 hour and chilled in an ice-bath, whereupon a rubbery mass of product deposited. Cold aqueous 1.0 M KOH (20 ml) was added, and 35 upon continued chilling the product solidified. The yellow-orange solid was broken-up, collected on a suction filter, rinsed with water and dried. The material (3.08 g) was crystallized from hot 95% ethanol (50 ml) to give 2.56 g (70.6% yield) of methyl 3,5-dinitro-4-(4′-ethoxyphenoxy)benzoate. Melting point: 101-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326402B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-76c460e71e2f4b6580260eff7906577f |
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| Source note | uspto-grants-2001_12 |
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