HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551916Generated: October 27, 2026
Hydrochloric Acid → (4-{[{4-[(4-Butylphenyl)ethynyl]benzyl}(ethylsulfonyl)amino]-methyl}phenoxy)acetic acid
https://huagongshe.com/reaction/551916
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl (4-{[{4-[(4-butylphenyl)ethynyl]benzyl}(ethylsulfonyl)-amino]methyl}phenoxy)acetate | HCID 11555583 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (4-{[{4-[(4-Butylphenyl)ethynyl]benzyl}(ethylsulfonyl)amino]-methyl}phenoxy)acetic acid | HCID 11627757 | 90% |
Reaction Steps
To a solution of methyl (4-{[{4-[(4-butylphenyl)ethynyl]benzyl}(ethylsulfonyl)amino]-methyl}phenoxy)acetate (7 mg, 0.013 mmol) in EtOH (1 mL) was added an aqueous solution of NaOH (20 μL, 5N). The reaction mixture was stirred at 70° C. for 2 hrs. Then an aqueous solution of HCl (1N) was added and extracted with EtOAc (2×). The combined organic layers were dried over Na2SO4 and the solvents were removed under reduced pressure to give 6 mg (90%) of the title compound as a pale yellow oil. HPLC, Rt: 5.0 min (purity: 75.0%). LC/MS, M+(ESI): 520.5, M−(ESI): 518.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947851B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-a878b99e8ca54aae8a21905140c2ed10 |
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| Source note | uspto-grants-2011_05 |
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