HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465821Generated: October 29, 2026
HCID 19815328, compound → HCID 19815363, compound
https://huagongshe.com/reaction/465821
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 19815328 | HCID 19815328 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 19815363 | HCID 19815363 | 87.5% |
Reaction Steps
A solution of 7.70 g of 1-[4-(2-carbomethoxyphenoxy)benzyl]-2-butyl-4-chloro-5-hydroxymethylimidazole in 250 mL of ethanol and 125 mL of 10% aqueous sodium hydroxide was refluxed for 5 hours. After cooling, the reaction mixture was filtered, and the solvent was removed in vacuo. The residue was dissolved in water, and the solution was acidified to pH 3.5 using hydrochloric acid. The precipitated solid was recovered by filtration and recrystallized from acetone to furnish 6.52 g of 2-butyl-4-chloro-1-[4-(2-carboxyphenoxy)benzyl]-5-hydroxymethylimidazole, m.p. 178°-180°. NMR (200 MHz, DMSO) δ7.79 (d, 1H); 7.53 (t, 1H); 7.23 (t, 1H); 7.07 (d, 2H); 6.94 (d, 1H); 6.87 (d, 2H); 5.18 (s, 2H); 4.32 (s, 2H); 2.47 (t, 2H); 1.46 (quint., 2H); 1.23 (sext., 2H); 0.78 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05153197 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-4000624e678d4676aecbf3aa3ba6dc2c |
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| Source note | uspto-grants-1992_10 |
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