HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → Benzenamine, 4-(2,6-diphenyl-4-pyridinyl)-N,N-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | 4-(Dimethylamino)Benzaldehyde | HCID 7479 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Benzenamine, 4-(2,6-diphenyl-4-pyridinyl)-N,N-dimethyl- | HCID 93126 | — |
Reaction Steps
75 parts of p-dimethylaminobenzaldehyde and 125 parts of acetophenone together with 500 parts of ammonium acetate are heated in 1,000 parts of glacial acetic acid for four hours under reflux. The precipitate deposited after standing for twelve hours at room temperature is suction filtered and recrystallized from 500 parts of ethanol. 57 parts of a pale yellow compound (2,6-diphenyl-4-(4'-dimethylaminophenyl)-pyridine) is obtained which has a melting point of 128° to 129° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985376 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-badc0423e2924a79b39b5765ab417922 |
| Source note | uspto-grants-1976_10 |