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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461728Generated: October 30, 2026

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

https://huagongshe.com/reaction/461728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantMethanone, [4-(bromomethyl)phenyl]-2-thienyl-HCID 12232971—
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 sufoxide 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 numberUS04064132
Source datasetuspto-grants-1977_12
ORD IDord-e6e1afaa1e5743caafbf3490ef9e5adb
Source noteuspto-grants-1977_12