HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547035Generated: October 31, 2026
Sodium Hydroxide → HCID 57709172, compound
https://huagongshe.com/reaction/547035
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 67065212 | HCID 67065212 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57709172 | HCID 57709172 | 58.7% |
Reaction Steps
A 2 N sodium hydroxide aqueous solution (0.50 mL, 1.0 mmol) was added to a solution of the mixture containing [4′-(1-ethyl-1-{4-[2-(1-hydroxy-cycloheptyl)-(E)-vinyl]-3-methyl-phenyl}-propyl)-2′-methyl-biphenyl-4-yl]-acetic acid methyl ester (14.0 mg) in methanol (1.0 mL), and the mixture was stirred with microwave heating at 100° C. for five minutes. An ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate and washing with brine. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate:methanol=100:0 to 90:10) to give the target compound as a colorless oil (8.0 mg, 19% in two steps).
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-3bc3e5bab32c4f6b961f50faf187ff02 |
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| Source note | uspto-grants-2011_05 |
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