HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-[4-[(5E)-5-Decen-1-yloxy]phenyl]-5-[(5,5,6,6,7,7,8,8,8-nonafluorooctyl)oxy]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-Decen-1-ol, (5E)- | HCID 5283292 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 4-[5-[(5,5,6,6,7,7,8,8,8-Nonafluorooctyl)oxy]-2-pyrimidinyl]phenol | HCID 135585897 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[4-[(5E)-5-Decen-1-yloxy]phenyl]-5-[(5,5,6,6,7,7,8,8,8-nonafluorooctyl)oxy]pyrimidine | HCID 23509149 | — |
Reaction Steps
A solution of DEAD (0.261 g, 1.50 mmol) in THF (20) was added dropwise to a stirred solution of 4-[5-(5,5,6,6,7,7,8,8,8-nonafluorooctyloxy)-pyrimidin-2-yl]-phenol (0.693 g, 1.50 mmol), trans-5-decen-1-ol (0.234 g, 1.50 mmol) and triphenylphosphine (0.399 g, 1.50 mmol) in THF (30) and the reaction mixture stirred at room temperature for 16 h. The solvent was removed in vacuo and the residues purified by column chromatography [silica gel, eluted with hexane/ethyl acetate (4:1)] to yield a colorless solid, which was recrystallized from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06759101B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-104789d05eba48a690decbce1e4e773a |
| Source note | uspto-grants-2004_07 |