Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Hydroperoxyphthalic acid | HCID 19809706 | — |
| Reactant | HCID 135500034 | HCID 135500034 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 135786536 | HCID 135786536 | 22% |
Reaction Steps
Monoperoxyphthalic acid, magnesium salt hexahydrate (1.4 g of a 80% pure solid, 0.0056 mole) is added portionwise to a 0° C. solution of (E)-2,6-bis(1,1-dimethylethyl)-4-[2-[5-(methylthio)-1,3,4-thiadiazol-2-yl]ethenyl]-phenol (1.0 g, 0.0028 mole) in methanol (15 ml) and water (7 ml). After the addition is complete the solution is allowed to warm to room temperature and stir for two hours. The mixture is then warmed on a steam bath for 45 minutes before cooling and concentrating in vacuo. The residue is dissolved in ether and washed with saturated aqueous NaHCO3, saturated aqueous NaCl, and dried over MgSO 4. Filtration and concentration in vacuo gives a residue which is purified by flash chromatography (SiO2) using a 15% ethyl acetate/hexane eluent, followed by recrystallization from ethyl acetate/hexane to give 0.22 g (1.1 g theor., 22%) (E)-2,6-bis(1,1-dimethylethyl)-4-[2- [5-(methylsulfonyl)-1,3,4-thiadiazol-2-yl]ethenyl]phenol, mp 235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05376670 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-47752102bebb4180a339b2e1df85b000 |
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| Source note | uspto-grants-1994_12 |
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