HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415492Generated: October 29, 2026
Hydrochloric Acid → HCID 44466336, compound
https://huagongshe.com/reaction/415492
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 44466333 | HCID 44466333 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44466336 | HCID 44466336 | — |
Reaction Steps
In a 15-mL round-bottom flask ethyl 2-(3,4-dichlorobenzyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxylate (0.46 mmol) was dissolved in a mixture of THF (2 mL) and MeOH (2 mL). Lithium hydroxide monohydrate (0.93 mmol) was dissolved in water (2 mL) and added to the reaction flask dropwise. The reaction mixture was stirred at room temperature for 6 hours, and then acidified with 1N aqueous HCl. The resulting mixture containing precipitate was poured into a separatory funnel and dichloromethane added until all precipitate dissolved (200 mL). The resulting solution was washed with water (50 mL) and dried over MgSO4. Concentration yielded 2-(3,4-dichlorobenzyl)-3-oxo-2,3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxylic acid as light-yellow precipitate. The final compound is more soluble in chloroform than dichloromethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088792B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-fa42c3c18c0c48bf8d937bbb8b96b16d |
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| Source note | uspto-grants-2012_01 |
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