HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 59406683, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3-Aminobenzyl alcohol | HCID 80293 | — |
| Reactant | HCID 59406765 | HCID 59406765 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59406683 | HCID 59406683 | — |
Reaction Steps
2.5 g (10 mmol) of 6-[4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-2H-pyridazin-3-one, 1.85 g (15 mmol) of 3-aminobenzyl alcohol and 3.9 g (15 mmol) of triphenylphosphine are suspended in 60 ml of THF under a nitrogen atmosphere, and the mixture is stirred at room temperature for 10 min. 2.9 g (15 mmol) of diisopropyl azodicarboxylate is then added dropwise over the course of 15 min. The reaction mixture is stirred at room temperature for 3 hours and subsequently evaporated. The residue is taken up in about 70 ml of 2-propanol, and the mixture is stirred for 15 minutes. The residue is filtered off with suction, washed well with 2-propanol, then with MTBE. The residue is dried in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367668B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-ddbff021131e416d9f1326c3ab1e1ed4 |
| Source note | uspto-grants-2013_02 |