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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408563Generated: October 25, 2026

Potassium Cyanide → 2-(1-Benzothiophen-2-yl)acetonitrile

https://huagongshe.com/reaction/408563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant2-(Chloromethyl)-1-benzothiopheneHCID 12813837—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product2-(1-Benzothiophen-2-yl)acetonitrileHCID 12631923—

Reaction Steps

To a solution of 2-chloromethyl-benzo[b]thiophene (1 eq.) in dioxane/water (2/1) was added KCN (1.5 eq.). The reaction was refluxed for 4 h. The crude was partitioned between water and EtOAc. The organic layer was washed with water, then brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc: 95/5 to 90/10) to afford benzo[b]thiophen-2-yl-acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-0ee2a227619148bfab509a57eefae68e
Source noteuspto-grants-2014_06