HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dimethylethyl 3-(difluoromethyl)-4-(phenylmethyl)-1-piperazinecarboxylate → tert-butyl 3-(difluoromethyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dimethylethyl 3-(difluoromethyl)-4-(phenylmethyl)-1-piperazinecarboxylate | HCID 67054946 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-butyl 3-(difluoromethyl)piperazine-1-carboxylate | HCID 67054906 | 97.1% |
Reaction Steps
10% Palladium on carbon (65 mg, 0.061 mmol) was added to a solution of tert-butyl 4-benzyl-3-(difluoromethyl)piperazine-1-carboxylate (0.20 g, 0.61 mmol, racemic from Step 3) in methanol (15 mL). The suspension was stirred under an atmosphere of hydrogen provided by a balloon. When the reaction showed no progress, 20% Pd(OH)2 on charcoal (47 mg, 0.061 mmol) was added and the suspension was shaken under 50-55 psi hydrogen for 2 h. The mixture was filtered and solvent removed in vacuo to afford product as a viscous oil (140 mg, 97%). 1H NMR (300 MHz, CDCl3): δ 5.90 (td, 0.1H), 5.52-5.12 (br s, 2H), 4.25-3.96 (br s, 1H), 3.94 (d, 1H), 3.27-2.77 (m, 4H), 1.45 (s, 9H); LCMS (M-tBu+2H)+: 181.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249145B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-f17f880a1b654bfd8f6dff5d2b553259 |
| Source note | uspto-grants-2016_02 |