HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 1,4-Bis(t-butoxycarbonyl)-2-(2-bromoethyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | di-tert-Butyl 2-(2-hydroxyethyl)piperazine-1,4-dicarboxylate | HCID 22710988 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,4-Bis(t-butoxycarbonyl)-2-(2-bromoethyl)piperazine | HCID 22710728 | — |
Reaction Steps
In methylene chloride (70 ml) were dissolved 1,4-bis(tert-butoxycarbonyl)-2-(2-hydroxyethyl)piperazine (2.01 g) and triphenylphosphine (1.98 g). Under ice cooling, carbon tetrabromide (3.07 g) was added to the resulting solution, followed by stirring at room temperature for 2.5 hours. The reaction mixture was extracted with a 10% aqueous solution of sodium thiosulfate. The organic layer was washed with saturated aqueous NaCl solution, dried over anhydrous sodium sulfate an distilled under reduced pressure to remove the solvent. The residue was subjected to column chromatography (hexane:ethyl acetate=4:1) using as a carrier silica gel, whereby the title compound (2.20 g) was obtained as colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06747023B1 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-39831b8d51d94294b2ce91658b8f3627 |
| Source note | uspto-grants-2004_06 |