Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,5-Di-tert-butyl-4-hydroxyhydrocinnamic acid hydrazide | HCID 64865 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ethyl orthoformate | HCID 31214 | — |
| Product | HCID 10447662 | HCID 10447662 | 774.4% |
Reaction Steps
A catalytic amount of p-toluenesulfonic acid (25 mg) is added to a stirring solution of 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoic acid hydrazide (0.50 g, 1.71 mmol) in triethyl orthoformate (10 mL). After 30 minutes, 10 mL of 1N hydrochloric acid is added, and stirring is continued for 30 minutes. The reaction mixture is diluted with ethyl acetate and washed twice with a saturated solution of sodium bicarbonate, twice with water, and once with brine. Drying the organic phase over magnesium sulfate and evaporation gives a crude product which is chromatographed on a column of silica with ethyl acetate/hexane (1/9 then 1/4) to afford 0.34 g (67%) of 2,6-bis(1,1-dimethylethyl)-4-[2-(1,3,4-oxadiazol-2-yl)ethyl]phenol, mp 100.0°-101.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102897 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-abf2a9f5881e4c1bb6a9a61cf65af418 |
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| Source note | uspto-grants-1992_04 |
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