HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-(4-(4-Pyridyl)piperazin-1-yl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-[4-(4-Pyridyl)piperazin-1-yl]anisole | HCID 14986902 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | 4-(4-(4-Pyridyl)piperazin-1-yl)phenol | HCID 14986903 | 95.6% |
Reaction Steps
The product from step (i) (1.5 g) in concentrated hydrobromic acid (30 ml) was heated under argon at 130°-135° C. for 21/2 hours. The solution was cooled, poured into water (150 ml) and basified with aqueous ammonia. The precipitate was filtered, washed with water and dried to give 4-[4-(4-pyridyl)piperazin-1-yl]phenol (1.36 g) as a solid: m.p. 310°-312° C.; NMR(d6DMSO) δ 8.2(2H,d); 6.8(4H,m); 6.66(2H,d); 3.45(4H,m); 3.08(4H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728701 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-9f122af1a0394a17b79d34afbf18a558 |
| Source note | uspto-grants-1998_03 |