HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631926Generated: October 30, 2026
Lithium Hydroxide → 5-(4-bromo-2-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid
https://huagongshe.com/reaction/631926
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 5-(4-bromo-2-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid ethyl ester | HCID 118062416 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(4-bromo-2-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid | HCID 118062573 | 100% |
Reaction Steps
In a 250 mL round-bottomed flask, 5-(4-bromo-2-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazole-4-carboxylic acid ethyl ester (291 mg, 887 μmol) was combined with tetrahydrofuran (18 mL) to give a colorless solution. 1M LiOH (9 mL, 9.00 mmol, Eq: 10.1) was added and the reaction was stirred at 25° C. for 15 h. The crude reaction mixture was concentrated in vacuo and acidified with 10 mL of 1M HCl. The reaction was diluted with EtOAc and the organic layer was washed with H2O (1×20 mL) and saturated NaCl (1×20 mL), dried over Na2SO4 and concentrated in vacuo. The white powder was dried under vacuum to afford 266 mg (100%) of the desired product. (M−H)−=297.8 and 299.9 (m/e).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321738B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-4c69b782ffbe4556a6f33622fc3b673d |
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| Source note | uspto-grants-2016_04 |
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