HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (3s, 5r)-1-(2,4-Dimethoxy-benzyl)-3,5-dimethyl-piperazin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3S, 5R)-1-(2,4-dimethoxy-benzyl)-3,5-dimethyl-4-trifluoroacetyl-piperazin-2-one | HCID 57171471 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (3s, 5r)-1-(2,4-Dimethoxy-benzyl)-3,5-dimethyl-piperazin-2-one | HCID 90816299 | 91% |
Reaction Steps
(3S, 5R)-1-(2,4-Dimethoxy-benzyl)-3,5-dimethyl-4-trifluoroacetyl-piperazin-2-one (575 mg, 1.54 mmol) is dissolved in 30 mL of methanol and 3 mL of H2O. Potassium carbonate (883 mg, 6.4 mmol) is added to the solution, and the reaction is refluxed for one and half hours before concentration. Ethyl acetate (3×50 mL) is used to extract the aqueous layer. Removal of Ethyl acetate afforded the crude amine (387 mg, 91% yield) as a clear oil. C15H22N2O3 MS m/z: 279.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612075B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-0dfd7411a8694bc0ac4aa37e7b0dabc9 |
| Source note | uspto-grants-2009_11 |