HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551900Generated: October 27, 2026
Hydrochloric Acid → 5-[{4-[(4-Butylphenyl)ethynyl]benzyl}(3-phenylpropyl)amino]-2-hydroxybenzoic acid, hydrochloride salt
https://huagongshe.com/reaction/551900
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-[{4-[(4-butylphenyl)ethynyl]benzyl}(3-phenylpropyl)amino]-2,2-dimethyl-4H-1,3-benzodioxin-4-one | HCID 11628259 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 5-[{4-[(4-Butylphenyl)ethynyl]benzyl}(3-phenylpropyl)amino]-2-hydroxybenzoic acid, hydrochloride salt | HCID 131728928 | 32% |
Reaction Steps
To a solution of 6-[{4-[(4-butylphenyl)ethynyl]benzyl}(3-phenylpropyl)amino]-2,2-dimethyl-4H-1,3-benzodioxin-4-one (147 mg, 0.26 mmol) in MeOH/THF (9 ml, (2/1)) was added an aqueous solution of NaOH (0.3 mL, 5N). The reaction mixture was stirred at rt for 48 hrs. Then a solution of HCl in MeOH (2.5 mL, 1.25M) was added and the solvents were 5 removed under reduced pressure. The residue was taken up with water (5 mL), extracted with Et2O (2×5 mL) and the combined organic layers were dried over Na2SO4. The solvent was removed under reduced pressure. The residue was dissolved in a solution of HCl in Et2O (2 mL, 1N). Evaporation of the solvent gave 60 mg (32%) of the title compound as a brown foam. HPLC, Rt: 4.8 min (purity: 78.1%). LC/MS, M+(ESI): 518.4, M−(ESI): 516.3.
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-53f19e1a5eda4c158094e31ccb4f2165 |
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| Source note | uspto-grants-2011_05 |
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