HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzyl-1-tert-butoxycarbonyl-2(S)-(2-methoxyethyl)piperazine → (S)-Tert-butyl 2-(2-methoxyethyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzyl-1-tert-butoxycarbonyl-2(S)-(2-methoxyethyl)piperazine | HCID 15406046 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | (S)-Tert-butyl 2-(2-methoxyethyl)piperazine-1-carboxylate | HCID 15406047 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 2, Step C, except using 4-benzyl-1-tert-butoxycarbonyl-2(S)-(2-methoxyethyl)piperazine (0.280 g, 0.83 mmol) and 10% palladium on carbon (80 mg). The title compound was obtained as an oil (179 mg). NMR (CD3OD, 300 MHz) δ 4.17 (1H, m), 3.81 (1H, dd, J=3, 13 Hz), 3.38 (2H, t, J=6 Hz), 2.82-3.02 (2H, m), 2.77 (2H, ABq, J=4, 13 Hz), 2.59 (1H, dt, J=4, 7 Hz), 2.04 (1H, m), 1.84 (1H, m), 1.46 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05736539 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-c1d9a9bdfe8d42d9b633ec544cf0328a |
| Source note | uspto-grants-1998_04 |