Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 54473706 | HCID 54473706 | — |
| Reactant | HCID 69892772 | HCID 69892772 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53845706 | HCID 53845706 | 70.7% |
Reaction Steps
To a solution in toluene (25 mL) of 4-bromomethyl-2-phenoxybenzoic acid methyl ester (3.37 g), prepared as in Example 157E, was added 18-crown-6 (0.52 g) and the potassium 3-pyridyloxide (2.20 g). The reaction mixture was heated at 70° C. for 1 hour during which time a black, insoluble tar formed. The reaction mixture was cooled to ambient temperature and diluted with toluene. The toluene was decanted from the tar and the tar was dissolved in 1:1 THF-water (20 mL). The aqueous THF was added to the toluene and the mixture was washed twice with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give a black oil. Chromatography on silica gel (1:1 ethyl acetate-hexanes) gave 4-(3-pyridyloxymethyl)-2-phenoxybenzoic acid methyl ester (2.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06693123B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-ad444eb570ec46ca8865252666baca82 |
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| Source note | uspto-grants-2004_02 |
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