HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-Tritylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Tritylpiperazine | HCID 11472931 | 23.2% |
Reaction Steps
To a solution of piperazine (25.9 g, 0.30 mol) in tetrahydrofuran (300 ml) at 0° C. was added triphenylmethyl chloride (27.9 g, 0.10 mol). The reaction was stirred for 48 hours at room temperature. The product was extracted from aqueous sodium carbonate with three portions of ether. The combined organic layers were washed with three portions of water, dried with sodium sulfate, and the volatiles were then evaporated. The residue was subjected to chromatography on silica (LPS-1) (eluting with 90:10:4 ether/acetonitrile/triethylamine) to yield 7.62 g of N-tritylpiperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576749 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-36d51ed950354c24a52cd00551ba5d02 |
| Source note | uspto-grants-1986_03 |