Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 59627760 | HCID 59627760 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59627762 | HCID 59627762 | — |
Reaction Steps
The 4′-methyl-5-(2-oxo-benzooxazol-3-yl)-biphenyl-3-carboxylic acid methyl ester from step 1 was dissolved in DMF (6 mL) and LiOH (500 mg, excess) was added. The reaction mixture was stirred at 120° C. overnight and then cooled to room temperature and partitioned between dichloromethane and saturated aqueous citric acid solution. The organic layer was concentrated under reduced pressure to give crude 4′-methyl-5-(2-oxo-benzooxazol-3-yl)-biphenyl-3-carboxylic acid, which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809402B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-a652c804ff0c45cb8b52e69277692ee5 |
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| Source note | uspto-grants-2014_08 |
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