HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → [(2S)-2-Methyl-1-piperazinyl]phenylmethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 57581556 | HCID 57581556 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [(2S)-2-Methyl-1-piperazinyl]phenylmethanone | HCID 57581475 | — |
Reaction Steps
(S)-tert-butyl 4-benzoyl-3-methylpiperazine-1-carboxylate (8.16 g, 26.8 mmol) was dissolved in dichloromethane (200 mL). Trifluoroacetic acid (20.7 ml) was added and the reaction was stirred at rt for 1.5 hours. The reaction was quenched into saturated K2CO3 (30 mL) and neutralized by the portion-wise addition of solid NaHCO3. The layers were separated and extracted twice with dichloromethane. The combined organics were dried (MgSO4) and evaporated to give a yellow oil. MS (M+H)+=205.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153633B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-cb30c2f8c58b427298c22302d42b8756 |
| Source note | uspto-grants-2012_04 |