HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650168Generated: October 30, 2026
Hydrochloric Acid → HCID 178479745, compound
https://huagongshe.com/reaction/1650168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178519558 | HCID 178519558 | — |
| Reactant | HCID 178524345 | HCID 178524345 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178479745 | HCID 178479745 | 58% |
Reaction Steps
2-hydroxy-3-[(1H-imidazol-4-yl)methyl]-benzoic acid (hydrochloride). 1 g of 2-hydroxy-3-[(1H-imidazol-4-yl)methyl]-benzenemethanol (prepared by the method described in Example 6.1 of the abovementioned U.S. patent application Ser. No. 116,325) is heated at 180° C. for two hours and a half and with thorough stirring, in the presence of 7.5 g of potassium hydroxide. The reaction mixture is then cooled and dissolved in 10 ml of water. The aqueous solution is acidified to pH 3-4 by addition of concentrated hydrochloric acid. The precipitate which separates is filtered off and dried, and is then extracted with boiling isopropyl alcohol. The isopropyl alcohol is then eliminated under reduced pressure, and the crystalline residue obtained is recrystallized in 5 ml of an 1N aqueous solution of hydrochloric acid. 0.74 g of 2-hydroxy-3-[(1H-imidazol-4-yl)methyl]-benzoic acid hydrochloride is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04923865 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-2db1afc458ff4c7fb48bd96b3b7fc47b |
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| Source note | uspto-grants-1990_05 |
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