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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267994Generated: October 27, 2026

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

https://huagongshe.com/reaction/1267994

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 numberUS06555555B1
Source datasetuspto-grants-2003_04
ORD IDord-7243b35117794728be52b947818d767e
Source noteuspto-grants-2003_04