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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650771Generated: November 1, 2026

Allyl Alcohol → HCID 14624408, compound

https://huagongshe.com/reaction/1650771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14624390HCID 14624390—
SolventEthyl AcetateHCID 8857—
ProductHCID 14624408HCID 1462440860%

Reaction Steps

To 20 ml of allyl alcohol, 0.4 g (0.008 mol) of 50% sodium hydride was added, and the mixture was stirred at room temperature for 30 minutes. Then, 2.8 g (0.008 mol) of 5-chloromethyl-3-(tert-butyl)-1-(2,4,6-trichlorophenyl)-1H-1,2,4-triazole was gradually added thereto under stirring at room temperature. After completion of the dropwise addition, the solution was heated and stirred under reflux for 2 hours. Then, 50 ml of ethyl acetate was added thereto, and the mixture was washed with water. The organic layer was dried, and the solvent was distilled off. The oily substance thereby obtained was purified by silica gel column chromatography to obtain 1.8 g (yield: 60.0%) of the desired compound as pale yellow prismatic crystals. Melting point: 34°-37° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925864
Source datasetuspto-grants-1990_05
ORD IDord-04df105e08a140ed8b390c11a388c95d
Source noteuspto-grants-1990_05