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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486971Generated: October 29, 2026

Ethyl acetate hexane → HCID 178506085, compound

https://huagongshe.com/reaction/1486971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl acetate hexaneHCID 21226206—
Reactant2,6-bis(trifluoromethyl)-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-1,2,4-triazol-3-yl)pyridineHCID 89401935—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
ProductHCID 178506085HCID 17850608558.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

In a 10 mL seal tube, 2,6-bis(trifluoromethyl)-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-1,2,4-triazol-3-yl)pyridine (2) (0.15 g, 1 eq.) was dissolved in dioxane HCl (5 mL) and seal tube was heated to 60° C. for 6 h. Reaction completion was monitored on TLC using ethyl acetate:hexane (5:5) as mobile phase. The reaction mixture was quenched into the ice-water NaHCO3 solution (50 mL) and was extracted with ethyl acetate (3×50 mL). Organic layer was washed with brine solution (3×50 mL). The organic layer was dried using anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to provide the 0.3 g of crude compound. The compound was purified by column chromatography using ethyl acetate/hexane as mobile phase. Compound was eluted out at 30% ethyl acetate in hexane to afford 4-(1H-1,2,4-triazol-3-yl)-2,6-bis(trifluoromethyl)pyridine (3) 0.060 g. Yield: 58.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428490B2
Source datasetuspto-grants-2016_08
ORD IDord-744e22b2f10c4749b8309de3e000c898
Source noteuspto-grants-2016_08