Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522455Generated: October 30, 2026

Acetonitrile → HCID 117899784, compound

https://huagongshe.com/reaction/522455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant1,6-DibromohexaneHCID 12368—
ReactantHCID 117899776HCID 117899776—
CatalystTetrabutylammonium BromideHCID 74236—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 117899784HCID 11789978497%

Reaction Steps

To 60 ml of acetonitrile were added 1.14 g (4.83 mmol) of 2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenol, 4.71 g (19.31 mmol) of 1,6-dibromohexane, 0.73 g (5.28 mmol) of potassium carbonate and catalytic amount of tetra-n-butylammonium bromide. The mixture was refluxed for 3 hours under heating. The mixture was allowed to cool to room temperature, and insoluble matters were removed by filtration. Then the solvent of filtrate was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=40:1˜20:1), to obtain 1.87 g (yield: 97%) of an intended product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09332754B2
Source datasetuspto-grants-2016_05
ORD IDord-16eb39d116c3448e8632179d372b2782
Source noteuspto-grants-2016_05