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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258917Generated: October 26, 2026

Sodium Cyanide → 2-[p-(2-Thenoyl)phenyl]acetonitrile

https://huagongshe.com/reaction/258917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantMethanone, [4-(bromomethyl)phenyl]-2-thienyl-HCID 12232971—
SolventDimethyl SulfoxideHCID 679—
Product2-[p-(2-Thenoyl)phenyl]acetonitrileHCID 12232974—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5.9 parts of sodium cyanide in 40 parts of dimethyl sulfoxide is heated to 60° C and there are added at once 11.3 parts of α-bromo-p-tolyl 2-thienyl ketone (exothermic reaction: temperature rises to 100° C). The whole is stirred for 2 hours at 60° C. After cooling, the reaction mixture is poured onto water and the product is extracted three times with 450 parts of chloroform. The combined extracts are washed twice with 200 parts of water, dried and evaporated. The dark-coloured residual tar is extracted several times with ether. The combined ether extracts are stirred with activated charcoal, filtered and evaporated. The residue is triturated in petroleumether (solid carbon dioxide) and the whole is evaporated, yielding 2-[p-(2-thenoyl)phenyl] acetonitrile as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035376
Source datasetuspto-grants-1977_07
ORD IDord-55bee046ecb64a8595f140947f9a1440
Source noteuspto-grants-1977_07