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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522447Generated: October 30, 2026

Hexane → 6-Thiocyanatohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl]ether

https://huagongshe.com/reaction/522447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium thiocyanateHCID 516872—
Reactant6-Bromohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl]etherHCID 117899737—
SolventEthanolHCID 702—
Product6-Thiocyanatohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl]etherHCID 11789969173%

Reaction Steps

In 30 ml of ethanol were added 1.51 g (3.43 mmol) of 6-bromohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl]ether and 1.67 g (17.2 mmol) of potassium thiocyanate. The mixture was refluxed for 3 hours under heating. The mixture was allowed to cool to room temperature, and the solvent was distilled off under reduced pressure. Then extraction was conducted by adding ethyl acetate and water. The organic phase obtained was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 1.04 g (yield: 73%) of an intended product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09332754B2
Source datasetuspto-grants-2016_05
ORD IDord-9ce77c7c910943bb9329a1a1028c6dbd
Source noteuspto-grants-2016_05