HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Benzyl 4-(piperidin-4-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyl 4-(1-(tert-butoxycarbonyl)piperidin-4-yl)piperazine-1-carboxylate | HCID 18971584 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Benzyl 4-(piperidin-4-yl)piperazine-1-carboxylate | HCID 57470863 | 111.1% |
Reaction Steps
To benzyl 4-(1-t-butoxycarbonylpiperidin-4-yl)piperazine 1-carboxylate (2.31 g) was added trifluoroacetic acid (10 ml) while cooling in an ice bath, followed by stirring at room temperature for 3 hr. The reaction mixture was poured into ice water, and a 5N aqueous solution of sodium hydroxide (26 ml) was added thereto. This was extracted with ethyl acetate:tetrahydrofuran=1:1. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was removed to provide the crude product of the titled compound as a pale yellow oil (1.93 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855290B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-ebd12f11d59442a59df8532c92243a10 |
| Source note | uspto-grants-2010_12 |