HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 89558677, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (4-iodo-2,5-dimethylpyrazol-3-yl)methanol | HCID 71307692 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89558677 | HCID 89558677 | 29% |
Reaction Steps
A mixture of (4-iodo-1,3-dimethyl-1H-pyrazol-5-yl)methanol (75 mg), 4-hydroxybenzotrifluoride (48 mg), 40% diisopropyl azodicarboxylate (90 mg, toluene solution), triphenylphosphine (117 mg) and tetrahydrofuran (3.0 mL) was stirred at a room temperature overnight. Thereafter, water was added to the reaction solution, and the obtained mixture was then extracted with ethyl acetate. The organic layer was washed with water, and was then dried over anhydrous sodium sulfate, followed by vacuum concentration. The residue was purified by column chromatography (silica gel cartridge, hexane/ethyl acetate=90:10 to 50:50), so as to obtain the title compound (34 mg) in the form of a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642626B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-37dbc81db86142bab320338b348b42bd |
| Source note | uspto-grants-2014_02 |