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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388266Generated: October 30, 2026

Potassium Cyanide → HCID 14293633, compound

https://huagongshe.com/reaction/388266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant1-Benzothiophene-2-carbaldehydeHCID 736500—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 14293633HCID 1429363346%

Reaction Steps

To a solution of benzo[b]thiophene-2-carbaldehyde (2.19 g, 13.5 mmol) in anhydrous THF (200 mL) was added a solution of NaHSO3 (6.18 g, 59.4 mmol) in water (50 mL). KCN (3.248 g, 49.9 mmol) was added and the mixture was stirred at room temperature for 22 hours. The reaction mixture was then heated at 45° C. for 1 hour. After cooling to room temperature, the mixture was diluted with water and brine and extracted with EtOAc three times. The combined organics were washed with brine, dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (0-25% EtOAc-hexanes) gave 2-(benzo[b]thiophen-2-yl)-2-hydroxyacetonitrile as an off-white solid (1.09 g, 46% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377930B2
Source datasetuspto-grants-2013_02
ORD IDord-e56f25395c9b4fac9f22eb5e34cf856f
Source noteuspto-grants-2013_02