Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Phenyl-1,3,4-oxadiazol-2-IN-5-one | HCID 352208 | — |
| Reactant | HCID 86733764 | HCID 86733764 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21521117 | HCID 21521117 | — |
Reaction Steps
40.5 g of 5-phenyl-1,3,4-oxadiazol-2-one (.25 mol) and 71 g of N,N-diethyl-dithiocarbamic acid (4-hydroxy-3,4-dimethylbenzyl) ester (0.25 mol) are dissolved in 500 ml of isopropanol at 60°C. After dropwise addition of 10 g of sodium hydroxide in 100 ml of water, the mixture is stirred for 9 hours at 60°C. The solvent is then largely evaporated off, the yellow residue is dissolved in acetonitrile, insoluble matter is filtered off and the mother liquor is again evaporated. The residue, which crystallises slowly, is recrystallised from methanol. 3-(3,5-Dimethyl-4-hydroxybenzyl)5-phenyl-1,3,4-oxadiazol-2-one (stabiliser No. 16) of melting point 135°C is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03971803 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-9f63cd4495554fff8c50e74e977c09e5 |
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| Source note | uspto-grants-1976_07 |
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