Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105974Generated: October 30, 2026

Benzaldehyde → 1,4-Bis(phenylglyoxaloyl)benzene

https://huagongshe.com/reaction/1105974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPotassium CyanideHCID 9032—
ReactantTerephthalaldehydeHCID 12173—
Product1,4-Bis(phenylglyoxaloyl)benzeneHCID 137905—

Reaction Steps

The benzoinic condensation of terephthalaldehyde (625 g) with benzaldehyde (2000 g) is effected in conditions strictly identical to those of example 1, while using 300 g of potassium cyanide, which represents 50% of the stoichiometrical proportion. The yield of pure bis-benzoin is 1516 g (94%). This product, when oxidized, yields 90% of very pure 1,4-bis (phenylglyoxyloyl) benzene. The tetraketone yield thus averages 85% with respect to the reacted terephthalic aldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04310699
Source datasetuspto-grants-1982_01
ORD IDord-8ac9f58f85ac4e93ac3fdd6eb45bcdd7
Source noteuspto-grants-1982_01