HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Benzyl piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyl tert-butyl piperazine-1,4-dicarboxylate | HCID 15016698 | — |
| Solvent | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | Benzyl piperazine-1-carboxylate | HCID 643495 | 159.6% |
Reaction Steps
N-tert-butyloxycarbonyl--N'-benzyloxycarbonyl-piperazine (1.8 g, 3.13 mmol) was dissolved in 10 mL of 4N-HCl/dioxane. It was stirred at room temperature for 30 minutes. The reaction mixture was cooled in an ice bath, 1N-NaOH solution was carefully added to the mixture to adjust pH above 10. Ethyl acetate (50 mL×3) was used to extract the compound. The combined ethyl acetate layers were washed with brine, dried over anhydrous sodium sulfate. After removal of the solvent, 1.1 g of N-benzyloxycarbonyl-piperazine was obtained in quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561140 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-f538866a62a94b3f87cb505e7e282844 |
| Source note | uspto-grants-1996_10 |