HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191690Generated: November 2, 2026
Methanol → 2-(4-Fluoroanilino)-4-((phenylthio)methyl)benzoic acid
https://huagongshe.com/reaction/2191690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-(4-fluoroanilino)-4-((phenylthio)methyl)benzoate | HCID 57667962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Fluoroanilino)-4-((phenylthio)methyl)benzoic acid | HCID 57667862 | 86.6% |
Reaction Steps
2.0 mol/L Sodium hydroxide aqueous solution 2.0 mL was added to a mixed solution of methanol 2.4 mL and tetrahydrofuran 2.4 mL of methyl 2-(4-fluoroanilino)-4-((phenylthio)methyl)benzoate 0.48 g, and it was stirred at room temperature for 17 hours. The solvent was removed under reduced pressure, ethyl acetate and water were added to it, and it was adjusted to pH4.0 with 1.0 mol/L hydrochloric acid. The organic layer was separated and collected,dried over anhydrous magnesium sulfate after washing with saturated sodium chloride aqueous solution, and the solvent was removed under reduced pressure. Hexane and diisopropyl ether were added to the obtained residue, and solid matter was filtrated to give 2-(4-fluoroanilino)-4-((phenylthio)methyl)benzoic acid 0.40 g of pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08327467B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-86fb27abc41547c6bc2912ea0ae66c1a |
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| Source note | uspto-grants-2012_12 |
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