HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389132Generated: November 1, 2026
Ethylene Glycol → HCID 58243619, compound
https://huagongshe.com/reaction/389132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 58243658 | HCID 58243658 | — |
| Product | HCID 58243619 | HCID 58243619 | — |
Reaction Steps
2-{1-[5-(2-bromo-4-fluorophenyl)-4-methyl-4H-1,2,4-triazol-3-yl]-1-methylethoxy}-5-chloro-benzonitrile (1.93 g) was suspended in ethyleneglycol (20 ml), and a 5M aqueous sodium hydroxide solution (4.3 ml) was added thereto, followed by stirring at 130° C. for 24 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 extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The resulting solid was washed with ethyl acetate to obtain 2-(1-{5-[2-bromo-4-(2-hydroxyethoxy)phenyl]-4-methyl-4H-1,2,4-triazol-3-yl}-1-methylethoxy)-5-chlorobenzoic acid (1.77 g) as a beige solid.
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-b3189917769e4f9ca2e6efdbaee93225 |
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| Source note | uspto-grants-2013_02 |
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