HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368489Generated: October 31, 2026
Aluminium lithium hydride → (1-(4-fluorophenyl)-2-((2,3,6-trifluorobenzyl)thio)-1H-imidazol-5-yl)methanol
https://huagongshe.com/reaction/2368489
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 1-(4-fluorophenyl)-2-((2,3,6-trifluorobenzyl)thio)-1H-imidazole-5-carboxylate | HCID 71117421 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Product | (1-(4-fluorophenyl)-2-((2,3,6-trifluorobenzyl)thio)-1H-imidazol-5-yl)methanol | HCID 71117330 | — |
Reaction Steps
To a solution of ethyl 1-(4-fluorophenyl)-2-((2,3,6-trifluorobenzyl)thio)-1H-imidazole-5-carboxylate (10) (1 g, 2.44 mmol) in THF at 0° C. was added lithium aluminum hydride (1M in THF, 4.88 mL, 4.88 mmol). The reaction was stirred for 1 h at 0° C. and at room temperature for 1 h. The solution was diluted with diethyl ether, and water (0.1 mL), 2N NaOH (0.1 mL), water (0.3 mL) and magnesium sulfate were added. The reaction was filtered and washed with THF to obtain (1-(4-fluorophenyl)-2-((2,3,6-trifluorobenzyl)thio)-1H-imidazol-5-yl)methanol (28) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703776B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-000a53afc9ea45feb4fc75480dc59165 |
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| Source note | uspto-grants-2014_04 |
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