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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant3-(2,6-Dichloro-phenyl)-5-trifluoromethyl-3H-[1,2,3]triazole-4-carboxylic Acid Ethyl EsterHCID 66704136—
SolventTetrahydrofuranHCID 8028—
Product[3-(2,6-Dichloro-phenyl)-5-trifluoromethyl-3H-[1,2,3]triazol-4-yl]methanolHCID 6670410797.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106077B2
Source datasetuspto-grants-2012_01
ORD IDord-facd9dea1d8c4a30ba9985adbcb35e4a
Source noteuspto-grants-2012_01