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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229355Generated: October 27, 2026

Trimethylsilyl cyanide → 6,7-Dihydrobenzo[b]thiophene-4-carbonitrile

https://huagongshe.com/reaction/2229355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4,5,6,7-Tetrahydro-4-oxothionaphtheneHCID 83418—
Catalystzinc(II)iodideHCID 9883512—
SolventAcetonitrileHCID 6342—
Product6,7-Dihydrobenzo[b]thiophene-4-carbonitrileHCID 22474132—

Reaction Steps

To a suspension of zinc iodide (6.2 g) in acetonitrile (200 ml) were added 4-keto-4,5,6,7-tetrahydrothianaphthene (20 g) and trimethylsilylcyanide (18 ml) successively. The mixture was stirred at room temperature for 5 hours. The reaction mixture was concentrated. The residue was dissolved in pyridine (65 ml), followed by adding phosphryl chloride (15 ml) dropwise at room temperature. The mixture was refluxed for 30 minutes. The reaction mixture was cooled with ice and thereto was added dropwise isopropanol. The reaction mixture was poured onto ice water and extracted with ethyl acetate. The extract was washed by hydrochloric acid, water and a saturated aqueous solution of sodium chloride successively, dried over anhydrous magnesium sulfate and concentrated to give the title compound (17 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420391B1
Source datasetuspto-grants-2002_07
ORD IDord-a6384d1ce26e400dbf1c406fa64f33e0
Source noteuspto-grants-2002_07