HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424811Generated: October 31, 2026
Diisobutylaluminum hydride → [3-(2,6-Dichloro-phenyl)-5-trifluoromethyl-3H-[1,2,3]triazol-4-yl]methanol
https://huagongshe.com/reaction/424811
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 3-(2,6-Dichloro-phenyl)-5-trifluoromethyl-3H-[1,2,3]triazole-4-carboxylic Acid Ethyl Ester | HCID 66704136 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-(2,6-Dichloro-phenyl)-5-trifluoromethyl-3H-[1,2,3]triazol-4-yl]methanol | HCID 66704107 | 97.3% |
Reaction Steps
To a 0° C. solution of 3-(2,6-dichloro-phenyl)-5-trifluoromethyl-3H-[1,2,3]triazole-4-carboxylic acid ethyl ester (28 g, 79 mmol) in THF (200 mL) is added dropwise 1M DIBAL (166 mL, 166 mmol) keeping the temperature below 5° C. After the addition, the bath is removed and the reaction is stirred for 18 h. The reaction is cooled to 0° C. and ether (300 mL) is added. The reaction is quenched with 1N HCl (250 mL) dropwise keeping the temperature below 15° C. The layers are separated and the water layer is washed with Ether (100 mL). The organics are combined and washed with water, brine, and dried with Na2SO4. The organic layer is concentrated to dryness to yield the title compound (24 g, 97%) and is used with no further purification. ES/MS m/e 312.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106077B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-facd9dea1d8c4a30ba9985adbcb35e4a |
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| Source note | uspto-grants-2012_01 |
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