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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269581Generated: October 31, 2026

Potassium Cyanide → HCID 54307398, compound

https://huagongshe.com/reaction/2269581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantHCID 54071145HCID 54071145—
ReactantHCID 54283396HCID 54283396—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 54307398HCID 54307398—

Reaction Steps

To 3-bromomethyl-4-(4-(methylthio)phenyl)-5-phenyl-thiophene-2-carboxylic acid methyl ester (1 g, prepared by using the same procedure described for 3-bromomethyl-5-(fluorophenyl)-4-(4-(methylthio)phenyl)thiophene-2-carboxylic acid methyl ester of Example 8, Step 2 but substituting benzaldehyde for 4-fluorobenz-aldehyde) in DMSO (25 mL) in an ice bath was added powdered KCN. The mixture was stirred for 15 minutes at R.T., then H2O was added and the mixture was extracted with Et2O (2X), the organic layers were combined, washed with brine, dried over MgSO4, filtered and the solvent was evaporated under vacuum. Purification by silica gel chromatography afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329421B1
Source datasetuspto-grants-2001_12
ORD IDord-2b12f7adc78d45a3996c8662e8d28778
Source noteuspto-grants-2001_12