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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995057Generated: October 31, 2026

Benzaldehyde → 3-Phenylpyrazin-2(1H)-one

https://huagongshe.com/reaction/1995057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantGlyoxalHCID 7860—
ReactantPotassium CyanideHCID 9032—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-Phenylpyrazin-2(1H)-oneHCID 155966—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of 0.3 mol. of potassium cyanide and 0.3 mol. of ammonium chloride in 100 ml. of water is added a solution of 0.3 mol. of benzaldehyde (Aldrich Chemical Co.) in 100 ml. of methanol. The reaction mixture is stirred at 25° C. for 6.0 hr. The oil layer is isolated and dissolved in methylene chloride. The solution is washed with water, dried and evaporated to give a brown oil. The oil is stirred with 150 ml. of concentrated hydrochloric acid for 1.0 hr. at 45° C. to precipitate phenylglycinamide hydrochloride. The precipitate is dissolved in 120 ml. of water stirred and cooled to 2° C. A solution of 4.8 g. (0.03 mol.) of 40% aqueous glyoxal is added, followed by dropwise addition of 6.0 ml. of 10 N sodium hydroxide. The reaction mixture is stirred for 5.0 hr. at 2° C. and then filtered. The filtrate is acidified to pH 6 with 3.0 ml. of 10 N hydrochloric acid and the precipitate of title compound is collected by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04402958
Source datasetuspto-grants-1983_09
ORD IDord-b967161755a14de985ee6f8a78251f6e
Source noteuspto-grants-1983_09