Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57879560 | HCID 57879560 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57879545 | HCID 57879545 | — |
Reaction Steps
1.2 mL of 2.0 mol/L aqueous sodium hydroxide was added to a suspension of 5 mL of methanol and 2.5 mL of dioxane containing 0.50 g of methyl 2-(benzamido)-4-phenylbenzoate at room temperature and stirred at 50° C. for 30 minutes. After the reaction mixture was cooled to room temperature, 1.0 mol/L hydrochloric acid was added to adjust to pH 3 and water and ethyl acetate were added. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure. Hexane was added to the obtained, residue and a solid substance was separated by filtration to obtain 0.36 g of 2-(benzamido)-4-phenylbenzoic acid as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07999132B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-43f2691bc05f49f48ff9a03ecb6205eb |
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| Source note | uspto-grants-2011_08 |
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