HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-Cyanobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | 4-(Aminomethyl)benzonitrile | HCID 82608 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Cyanobenzaldehyde | HCID 66042 | 60% |
Reaction Steps
7.9 g of p-cyanobenzylamine, 8.4 g of hexamethylenetetramine, 40 ml of water, 20 ml of acetic acid and 50 ml of toluene were mixed and reacted at 90° C. for 2 hours while stirring. The reaction solution was cooled to room temperature and the toluene layer was separated, washed with water and concentrated until crystals were precipitated. The concentrated toluene solvent was placed in water, the toluene was removed by azeotropic distillation, and the residue was cooled to room temperature. The crystals precipitated were collected by filtration, washed with water and dried to obtain 4.8 g (yield: 60%) of p-cyanobenzaldehyde. The purity was 99.5% or more.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262292B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-07531a4b9ccf4750b6836ba5342d02ba |
| Source note | uspto-grants-2001_07 |