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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522439Generated: October 29, 2026

Acetonitrile → HCID 117899761, compound

https://huagongshe.com/reaction/522439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-5-chloropentaneHCID 96070—
ReactantHCID 117899720HCID 117899720—
CatalystTetrabutylammonium BromideHCID 74236—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 117899761HCID 11789976180.7%

Reaction Steps

To 100 ml of acetonitrile were added 2.5 g (11 mmol) of 4-methyl-3-(2,2,2-trifluoroethylthio)phenol, 2.5 g (13 mmol) of 1-bromo-5-chloropentane, 1.9 g (14 mmol) of potassium carbonate and 0.35 g (1.1 mmol) of tetra-n-butylammonium bromide. The mixture was refluxed for 5 hours under heating and then allowed to cool to room temperature. 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 2.9 g (yield: 79%) of an intended product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09332754B2
Source datasetuspto-grants-2016_05
ORD IDord-80f5a2f55d7d49b6851967cd8a3a2076
Source noteuspto-grants-2016_05