HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → {4-[5-(4-Isobutylphenyl)-1,3,4-oxadiazol-2-yl]phenyl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]-5-(4-isobutylphenyl)-1,3,4-oxadiazole | HCID 59204284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | {4-[5-(4-Isobutylphenyl)-1,3,4-oxadiazol-2-yl]phenyl}methanol | HCID 59204276 | 88.5% |
Reaction Steps
Tetrabutylammonium fluoride (1.0 M in THF, 2.0 mL) was added to a solution of 2-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]-5-(4-isobutylphenyl)-1,3,4-oxadiazole (0.50 g, 1.18 mmol) and THF (10 mL) and stirred at room temperature for 16 hours. The reaction mixture was diluted with ethyl acetate (100 mL), washed with water and brine, dried (Na2SO4,), filtered and concentrated in vacuo to give the title compound (0.322 g, 88% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07671043B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-b18b14a2adc740f8bcc93019f46efd5f |
| Source note | uspto-grants-2010_03 |