HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-Boc-2-methyl-1-phenylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (+/-)-tert-Butyl 3-methyl-4-(4-aminophenyl)piperazine-1-carboxylate | HCID 22633057 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Phosphinic Acid | HCID 4124402 | — |
| Product | 4-Boc-2-methyl-1-phenylpiperazine | HCID 22633071 | — |
Reaction Steps
To a solution of (±)-tert-butyl 3-methyl-4-(4-aminophenyl)piperazine-1-carboxylate (325 mg) in 50% hypophosphorous acid (1.27 ml) containing copper(I) oxide (8.0 mg) was added dropwise a solution of sodium nitrite (92 mg) in water (2 ml) at 0° C. with stirring. After 2 hours, the reaction mixture was made alkaline with 40% NaOH solution and extracted with ethyl acetate twice. The organic layers were combined and washed with water and brine. The solvent was evaporated, and the residue was purified by silica gel column chromatography (hexane-ethyl acetate 1:1) to give the title compound in a pure form as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825200B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-af3dad8bbe5a48e8995131070a264a16 |
| Source note | uspto-grants-2004_11 |