HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 117966963, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 2-[4-(Trifluoromethoxy)phenyl]ethanol | HCID 10750766 | — |
| Reactant | HCID 117899631 | HCID 117899631 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117966963 | HCID 117966963 | 40.1% |
Reaction Steps
In 30 ml of tetrahydrofuran were dissolved 0.3 g (1.19 mmol) of 2,4-dimethyl-5-(2,2,2-trifluoroethylsulfinyl)phenol, 0.29 g (1.41 mmol) of 2-(4′-trifluoromethoxyphenyl)ethanol and 0.41 g (1.56 mmol) of triphenylphosphine. Thereto was added 0.31 g (1.53 mmol) of diisopropyl azodicarboxylate at room temperature, and stirred for 16 hours. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=5:1), and the residue was washed with n-hexane, to obtain 0.21 g (yield: 40%) of an intended product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09332754B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-4465b8af0b494552a868cd7d1b492ab5 |
| Source note | uspto-grants-2016_05 |