HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547020Generated: November 1, 2026
Sodium Hydroxide → HCID 57708929, compound
https://huagongshe.com/reaction/547020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (4'-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-biphenyl-3-yl)-acetic Acid Methyl Ester | HCID 57709149 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 57708929 | HCID 57708929 | 79.2% |
Reaction Steps
A 1 N sodium hydroxide aqueous solution (0.185 mL, 0.185 mmol) was added to a solution of (4′-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-biphenyl-3-yl)-acetic acid methyl ester (Example 124-(1); 30.8 mg, 0.062 mmol) in methanol-tetrahydrofuran (1:1, 3 mL), and the mixture was stirred at room temperature for three days. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution, followed by extraction with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (chloroform:methanol=10:1) to give the target compound as a colorless oil (23.8 mg, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935688B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-1ab05105df61485995413bcfb6cf7198 |
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| Source note | uspto-grants-2011_05 |
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