HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389129Generated: October 30, 2026
Ethylene Glycol → HCID 58244020, compound
https://huagongshe.com/reaction/389129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 58243848 | HCID 58243848 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58244020 | HCID 58244020 | — |
Reaction Steps
Potassium hydroxide (87 mg) was added to a mixture of 3-bromo-4-[(1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}cyclopropyl)oxy]benzamide (250 mg) and ethyleneglycol (6 ml), followed by stirring at 130° C. for 3 hours. The reaction solution was cooled to room temperature, and water was added thereto, followed by washing with ethyl acetate. The aqueous layer was acidified with 1M hydrochloric acid and then extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting product was solidified with diisopropylether and washed to obtain, as a colorless solid, 3-bromo-4-[(1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}cyclopropyl)oxy]benzoic acid (71 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377923B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-e9e0fc26b4bb480a8838d3a43c2deacb |
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| Source note | uspto-grants-2013_02 |
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