HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 53954443, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-(Dimethylamino)Benzaldehyde | HCID 7479 | — |
| Reactant | Octyl Acetate | HCID 8164 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53954443 | HCID 53954443 | 93.6% |
Reaction Steps
Sodium hydride (1.9 g of an 80% dispersion in oil) was added portionwise with stirring over 0.5 hour to 4-dimethylaminobenzaldehyde (7.46 g) in 1-octyl acetate (158 g) at 25° C. The temperature was raised until a steady evolution of hydrogen was observed (40° C.) and held at this temperature for 48 hours. The cooled mixture was treated with glacial acetic acid (4 ml) and then water (50 ml) added. The upper layer was separated, washed with 10% sodium carbonate solution, water, and dried (MgSO4). The excess 1-octyl acetate was removed by distillation at 15 mm pressure. the residue solidified on cooling. It was crystallised from petroleum ether (B.P. 40°-60°) at 0° C., giving 14.2 g pale yellow crystals, m.p. 48°-49.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04592906 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-4e38d47174184020a52dbad2bfb02039 |
| Source note | uspto-grants-1986_06 |