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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650168Generated: October 30, 2026

Hydrochloric Acid → HCID 178479745, compound

https://huagongshe.com/reaction/1650168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178519558HCID 178519558—
ReactantHCID 178524345HCID 178524345—
SolventWaterHCID 962—
ProductHCID 178479745HCID 17847974558%

Reaction Conditions

Temperature180 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923865
Source datasetuspto-grants-1990_05
ORD IDord-2db1afc458ff4c7fb48bd96b3b7fc47b
Source noteuspto-grants-1990_05