HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → {4-[3-(4-Isobutylphenyl)-1,2,4-oxadiazol-5-yl]phenyl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | N'-{[4-(Hydroxymethyl)benzoyl]oxy}-4-isobutylbenzenecarboximidamide | HCID 72530370 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | {4-[3-(4-Isobutylphenyl)-1,2,4-oxadiazol-5-yl]phenyl}methanol | HCID 59204309 | 46% |
Reaction Steps
Tetrabutylammonium fluoride (1.0 M solution in THF, 10 mL) was added to a solution of N′-{[4-(hydroxymethyl)benzoyl]oxy}-4-isobutylbenzenecarboximidamide (3.07 g, 9.42 mmol) and THF (50 mL) and stirred at room temperature for 20 hours. The reaction mixture was diluted with ethyl acetate, washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo to give the title compound (1.33 g, 46% yield) as a crude solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07671043B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-97fc3b451b06416d830a757cdf6a8469 |
| Source note | uspto-grants-2010_03 |