HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606246Generated: October 31, 2026
4-Cyanobenzaldehyde → HCID 21388866, compound
https://huagongshe.com/reaction/1606246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Alumina | HCID 9989226 | — |
| Reactant | HCID 21388859 | HCID 21388859 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21388866 | HCID 21388866 | — |
Reaction Steps
A mixture of 0.835 g. of p-methoxycarbonyloxyaniline and 0.655 g. of p-cyanobenzaldehyde is gassed with argon in 50 ml. of benzene and heated under reflux for 1 hour (bath temperature 130°). The resulting water is separated with a water separator. During an additional hour, benzene condensed in the reflux condenser is now passed back into the reaction vessel through a layer of 20 g. of aluminium oxide (act. I). After cooling, the reaction mixture is freed from solvent in vacuum at 50°C. bath temperature, whereby there remain 1.395 g. of yellowish crystals which are recrystallized several times from isopropanol up to constant melting point and clearing point and up to the disappearance of side-products in the gas chromatogram. The pure, slightly yellowish p-[(p-cyanobenzyliden)amino]phenyl methyl carbonate obtained has a melting point of 145.1°-146.2° and a clearing point of 163.4°. UV (EtOH): ε270 = 20,250, ε324 = 10,800 (shoulders at 243 and 221 nm; minima at 312 and 233 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03952046 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-58ddcc5add7f436ba9281604706439e9 |
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| Source note | uspto-grants-1976_04 |
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