HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 118161858, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | (1-methyl-1H-imidazol-4-yl)methanol | HCID 7060524 | — |
| Reactant | HCID 178518982 | HCID 178518982 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118161858 | HCID 118161858 | 30.3% |
Reaction Steps
Diisopropylazodicarboxylate 40% solution in toluene (0.27 mL, 0.51 mmol) was added under stirring to a solution of 5-(4-(trifluoromethoxy)phenyl)benzo[d]isoxazol-3-ol (100 mg, 0.34 mmol), triphenylphosphine on resin (3 mmol/g) (330 mg, 1 mmol), and 1-methylimidazol-4-yl methanol (60 mg, 0.51 mmol) in THF. The reaction mixture was stirred at ambient temperature overnight. Volatiles were evaporated under vacuum and the residue was purified on 12 g silica gel with 0-20% methanol in dichloromethane and gave the title compound (40 mg, 0.103 mmol) as yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09416115B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-776e0eddcccb43e08b4ff2cf870fa24b |
| Source note | uspto-grants-2016_08 |