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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570032Generated: October 30, 2026

Ethylenediamine → 3-Phenyl-1,4,5,6-tetrahydropyrazine-2-carbonitrile

https://huagongshe.com/reaction/570032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantSodium CyanideHCID 8929—
ReactantPhenylglyoxalHCID 14090—
ReactantSodium BisulfiteHCID 23665763—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Phenyl-1,4,5,6-tetrahydropyrazine-2-carbonitrileHCID 1360892254%

Reaction Conditions

Temperature50 °C

Reaction Steps

13.8 parts of phenylglyoxal and 40 parts by volume of water are initially taken and heated to about 50° C., 61 parts of 38% strength aqueous NaHSO3 solution are introduced, and methanol is added in an amount sufficient to dissolve virtually all solid material. Thereafter, 6 parts of ethylenediamine are added at about 30° C., the mixture is heated at 50° C. for 30 minutes and then cooled to about 10° C., a solution of 5.2 parts of 95% pure NaCN in 13 parts by volume of water is added at this temperature, stirring is continued for a further 2 hours at room temperature and working up is carried out as described under Example 4. 10 parts (54% of theory) of 1,4,5,6-tetrahydro-3-phenyl-2-cyanopyrazine are obtained in the form of a reddish brown, viscous oil. The mass spectrum of this product shows the molecular peak expected for the empirical formula C11H11N3, at e/m=185, and its NMR spectrum exhibits the bands typical of the different NH groups, at about 3.5 ppm (N1 -H) and about 6.15 ppm (N4 -H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734499
Source datasetuspto-grants-1988_03
ORD IDord-271a8c3dce49462ea99cf70ef5d32c70
Source noteuspto-grants-1988_03