HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178482859, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N,N-dimethyl-p-phenylenediamine | HCID 7472 | — |
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178482859 | HCID 178482859 | 73.5% |
Reaction Steps
To a mixture of 4-chloro-benzaldehyde (1.55 g, 11.0 mmol) and N,N-dimethyl-benzene-1,4-diamine (1.5 g, 11.0 mmol) in EtOH (15 ml) was added a catalytic amount of AcOH (0.063 ml, 1.1 mmol) at RT. The reaction mixture was heated at reflux and stirred for 14 h during which time precipitation took place. After cooling to RT, the slurry was filtered and washed with heptane. The solid was collected and dried under high vacuum to yield the title compound (2.09 g, 8.08 mmol, 73%) as a brownish solid. 1H NMR (400 MHz, CDCl3): 3.01 (s, 6H), 6.78 (m, 2H), 7.29 (m, 2H), 7.44 (m, 2H), 7.84 (m, 2H), 8.49 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09051279B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-a9ba4adcc7754259980a87f577438f01 |
| Source note | uspto-grants-2015_06 |