HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → [4-(4-Methyl-piperazin-1-yl)-phenyl]-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dibenzyl diselenide | HCID 95955 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,2,2-Trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanol | HCID 68277172 | — |
| Product | [4-(4-Methyl-piperazin-1-yl)-phenyl]-acetic acid | HCID 28807075 | — |
Reaction Steps
0.559 g (14.77 mmol) of sodium borohydride is added quickly to 2.294 g (7.35 mmol) of dibenzyl diselenide in 28 ml of ethanol. The reaction mixture is stirred at room temperature for 1 hour. 2.266 g (7 mmol) of 2,2,2-trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanol and 1.680 g (42.0 mmol) of sodium hydroxide are then added. The reaction mixture is stirred at 35° C. for 24 hours. The solvent is concentrated and the crude product extracted with ethyl acetate after adding a pH 5 aqueous phase. The organic phases are combined, dried on magnesium sulfate and then concentrated to yield 2-(4-(4-methylpiperazine-1-yl)phenyl)acetic acid which is used without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09381195B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-1cf5ad2b3e3f4b46a07e3d3f89283128 |
| Source note | uspto-grants-2016_07 |