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): δ 9.26 (s, 1H), δ 8.15 (m, 2H), δ 8.06 (d, 2H), δ 7.62 (m, 3H), δ 7.07 (d, 2H); mp 256.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495644B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-0e86bc0c269d4755892bb090ecfd7e2b |
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| Source note | uspto-grants-2002_12 |
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