HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 67608705, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3,4-Difluorophenol | HCID 75927 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 67606706 | HCID 67606706 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 67608705 | HCID 67608705 | 80% |
Reaction Steps
A solution of alcohol 77 (0.84 g, 2.2 mmol) in benzene (15 mL) was treated with 3,4-difluoro-phenol (402 mg, 3.1 mmol) and triphenylphosphine (864 mg, 3.3 mmol). To this solution was added DIAD (0.65 mL, 3.3 mmol) and the reaction mixture was stirred at ambient temperature. After 16 h, the solution was concentrated, diluted with DCM, washed with 1M NaOH, dried over anhydrous Na2SO4, filtered and concentrated. The aqueous phase was back-extracted with Et2O and the combined organic extracts were absorbed on SiO2 and purified by flash chromatography (3:1 hexane/EtOAc to 1:1 hexane/EtOAc) to afford 78 (0.86 g) which was contaminated with DIAD-related impurities and used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415486B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-48e48c6edba647ef84a637d0b34a2718 |
| Source note | uspto-grants-2013_04 |