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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546766Generated: October 31, 2026

Tetracyanoethylene → HCID 66839327, compound

https://huagongshe.com/reaction/546766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetracyanoethyleneHCID 12635—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 66839257HCID 66839257—
SolventAcetonitrileHCID 6342—
ProductHCID 66839327HCID 66839327—

Reaction Steps

A solution containing 1-[bis-(2-chloroethoxy)methyl]-4-fluorobenzene (5.43 g), trimethylsilyl cyanide (4.06 mL) and tetracyanoethylene (520 mg) in acetonitrile (100 mL) was heated under reflux for four hours. The reaction solution was returned to room temperature and the solvent was evaporated under reduced pressure. Ethyl acetate and brine were added to the residue, and the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (carrier: Chromatorex, elution solvent: heptane/ethyl acetate) to obtain the title compound (4.3 g). The property values of the compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935815B2
Source datasetuspto-grants-2011_05
ORD IDord-c06382617f5b4bae89642252df053480
Source noteuspto-grants-2011_05