HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466397Generated: October 29, 2026
HCID 19815285, compound → HCID 19815439, compound
https://huagongshe.com/reaction/466397
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 19815285 | HCID 19815285 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 19815439 | HCID 19815439 | 82.8% |
Reaction Steps
A solution of 0.30 g of 1-[(3'-carbomethoxybiphenyl-4-yl)methyl]-2-butyl-4-chloro-5-hydroxymethylimidazole in 16 mL of ethanol and 8 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 aqueous ethanol to furnish 0.24 g of 1-[(3'-carboxybiphenyl-4-yl)methyl]-2-butyl-4-chloro-5-hydroxymethylimidazole (m.p. 180°-181°); NMR (200 MHz, DMSO-d6): δ 8.26 (s, 1H); 8.04 (d, 1H); 7.77 (d, 1H); 7.52 (t, 1H); 7.36 (A2M2, 4H); 5.30 (s, 2H); 4.48 (s, 2H); 2.57 (t, 2H); 1.64 (quint., 2H); 1.34 (sext., 2H); 0.87 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155118 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-e6d7ba5a327a429ba33b51176ded23a0 |
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| Source note | uspto-grants-1992_10 |
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