HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454576Generated: October 29, 2026
Hydrochloric Acid → 2-(2-Hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoic acid
https://huagongshe.com/reaction/454576
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoate | HCID 58508867 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2-Hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoic acid | HCID 58508448 | 33.8% |
Reaction Steps
A 2.0 mol/L aqueous solution of sodium hydroxide (0.33 mL) was added to a methanol (2.0 mL) suspension of the obtained methyl 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoate (0.058 g), followed by stirring at 60° C. for 9 hours and 20 minutes. The reaction mixture was cooled to room temperature, and 6 mol/L hydrochloric acid (0.11 mL) was added thereto. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 95-85% chloroform/methanol] to obtain 0.019 g of 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492582B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-d817427eb2b5422ca232ca8dacbf2642 |
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| Source note | uspto-grants-2013_07 |
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