Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | HCID 69882730 | HCID 69882730 | — |
| Product | 23133-34-8 | HCID 745192 | — |
Reaction Steps
3.5 g (13.89 mmol) of 2-(p-anisoyl)5-phenyl 1,3,4-oxadiazole and 100 mL of concentrated HI aqueous solution was mixed under nitrogen and refluxed at 130° C. for 12 hours. The mixture was cooled down to room temperature and 100 mL of deionized water was added. The precipitate was collected by filtration and dried under vacuum, p-(5-phenyl-1,3,4-oxadiazole-2-yl) phenol was obtained. 1H-NMR (acetone-d6, ppm) δ9.26 (s, 1H), δ8.15 (m, 2H), δ8.06 (d, 2H), δ7.62 (m, 3H), δ7.07 (d, 2H); mp 256.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06693158B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-8e5a2e8e986e445bafa2f0fc12ff41b3 |
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| Source note | uspto-grants-2004_02 |
|---|