Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 86584668 | HCID 86584668 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | HCID 23441961 | HCID 23441961 | — |
Reaction Steps
To 5-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzene-1,3-dicarboxylic acid, diethyl ester (0.97 g, 2.0 mmol) in tetrahydrofuran/water (20 mL, 1/1) was added lithium hydroxide (0.42 g, 10 mmol). After heating at 60° C. for 90 minutes, the material was partitioned between ethyl acetate and 2 N HCl. The organic layer was separated, dried (MgSO4), and the solvent removed in vacuo to give 5-[(6-(3-cyanophenoxy)-3,5-difluoro-4-methylpyridin-2-yl)oxy]benzene-1,3-dicarboxylic acid; NMR (DMSO) 8.25 (s, 1), 7.85 (s, 2), 7.4-7.7 (m, 3), 7.3 (m, 3), 2.4 (s, 3) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479485B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-db0c89954052476d9104931d44c06b6e |
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| Source note | uspto-grants-2002_11 |
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