HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Methoxyphenyl)piperazine → 1-(2-methoxy-5-nitrophenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1-(2-methoxy-5-nitrophenyl)piperazine | HCID 3783138 | 76.2% |
Reaction Steps
Potassium nitrate (6.06 g) was added portionwise during 2 h to a solution of 1-(2-methoxyphenyl)piperazine ( 10.0 g) in sulphuric acid (50 ml; 95%) at room temperature. The resulting brown solution was stirred at room temperature for 30 min and added cautiously to ice (300 ml). The solution was basified with aqueous sodium hydroxide (5N) and extracted with ethyl acetate (2×400 ml). The dried extract was evaporated and the residue was purified on a column of silica (190:10:1) to give the title compound as a yellow solid (9.4 g). m.p. 102°-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05358948 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-8773250e295742a6b3e08e7a700fe625 |
| Source note | uspto-grants-1994_10 |