HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770198Generated: November 1, 2026
Hydrochloric Acid → HCID 178496783, compound
https://huagongshe.com/reaction/1770198
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 178509731 | HCID 178509731 | — |
| Product | HCID 178496783 | HCID 178496783 | — |
Reaction Steps
A suspension of 19.9 g (0.1 mole) of 2-hydroxy-3-(1H-imidazol-4-ylmethyl)-benzonitrile (prepared in example 1.1 above) in 600 ml of methanol, cooled to 10° C., is saturated with gaseous hydrochloric acid. 60 ml of water are added, the suspension is cooled to -25° C. and is saturated once again with gaseous hydrochloric acid. The reaction mixture is kept at that temperature for 15 hours. The solution is evaporated and the residue is taken up in 500 ml of ice-cold water; the resulting suspension is neutralized with an aqueous sodium bicarbonate solution. The solution is extracted 4 times with 250 ml of ethyl acetate and the organic phases are combined. The organic phase is washed with 200 ml of a saturated aqueous sodium chloride solution, is then dried over magnesium sulfate, filtered and evaporated. 19.1 g of methyl 2-hydroxy-3-(1H-imidazol-4-ylmethyl-)benzenecarboximidate are obtained which are used as such in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05385927 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-2d2a1bd63eea4cb09d4b37f4cb52f517 |
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| Source note | uspto-grants-1995_01 |
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