HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 1,4-Bis(phenylglyoxaloyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Terephthalaldehyde | HCID 12173 | — |
| Product | 1,4-Bis(phenylglyoxaloyl)benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310699 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-8ac9f58f85ac4e93ac3fdd6eb45bcdd7 |
| Source note | uspto-grants-1982_01 |