HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-[5-(4-Methoxy-benzenesulfonyl)2-methoxy-phenyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Methoxy-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonyl chloride | HCID 12136655 | — |
| Reactant | HCID 178491912 | HCID 178491912 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[5-(4-Methoxy-benzenesulfonyl)2-methoxy-phenyl]piperazine | HCID 9968960 | 36% |
Reaction Steps
To a solution of 4-methoxy-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonyl chloride (0.19 g), prepared as in Example 1 Step 2, in THF (0.5 ml) at 0° C. under argon atmosphere was added dropwise a solution of 4-methoxyphenylmagnesium bromide in THF (0.5M, 2 ml; 1 mmol). After stirring at this temperature for 1 h. A solution of 6N NaOH (0.5 ml) was added and the reaction mixture was stirred at ambient temperature for 20 h. Water was added (10 ml) and the mixture was extracted into ethyl acetate (20 ml). The organic phase was dried (Na2SO4) and concentrated in vacuo to give 1-[5-(4-methoxy-benzenesulfonyl)2-methoxy-phenyl]piperazine as a white solid (0.65 g, 36%), MS, MH+ 363.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825202B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-749f4815bc714a1d877f34835426b867 |
| Source note | uspto-grants-2004_11 |