HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 13796483, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Benzaldehyde, 4-octyl- | HCID 2734685 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 13796483 | HCID 13796483 | — |
Reaction Steps
A mixture of 5.9 g. of p-aminobenzonitrile and 10.9 g. of p-n-octylbenzaldehyde in 100 ml. of benzene is treated with 150 ml. of p-toluenesulfonic acid and reacted as described in Example 1. After evaporation, there remain 16.5 g. of a yellow oil which crystallizes with cooling. Purification is carried out by several recrystallizations from isopropanol as described in Example 1. The p-[(p-n-octylbenzyliden)amino]benzonitrile which is obtained has a melting point of 32.5°-32.8° C. and a clearing point of 68.8° C. Up to 54.4° C. the compound is smectic. UV (ethanol): ε280 = 24200 (shoulder at 312 nm). The nuclear magnetic resonance, mass spectrum, infrared and microanalysis data confirm the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04058477 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-e90d1dd01b02444ca2ae986dea3642f4 |
| Source note | uspto-grants-1977_11 |