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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868508Generated: October 30, 2026

Benzaldehyde → Mandelonitrile

https://huagongshe.com/reaction/868508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium CyanideHCID 9032—
SolventWaterHCID 962—
ProductMandelonitrileHCID 10758—

Reaction Steps

A 500 ml four-neck round bottom flask was equipped with a magnetic stirring bar, water condenser, addition funnel and drying tube. The glassware was dried and to this was charged 21.2 grams (0.2 mole) benzaldehyde and 19.5 grams (0.3 mole) potassium cyanide dissolved in 70 ml of water. The reaction flask was cooled to 10°-15° C. using a water/ice bath. To this was added 70 ml of 40% sulfuric acid over a 60 minute period. After the addition was complete, the reaction was allowed to warm to room temperature and stir for an additional two hours. At the end of this time the reaction mixture was extracted with carbon tetrachloride (3×75 ml), washed the combined carbon tetrachloride layers with water (2×50 ml), dried the carbon tetrachloride layer with anhydrous magnesium sulfate, filtered and concentrated to yield benzaldehyde cyanohydrin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04780458
Source datasetuspto-grants-1988_10
ORD IDord-64c421b95df24080ad1ec947637b0132
Source noteuspto-grants-1988_10