Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | HCID 136401346 | HCID 136401346 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135503589 | HCID 135503589 | — |
Reaction Steps
To a solution of 2.6 g (0.044 mole) of guanidine in absolute ethanol (100 ml) is added dropwise a solution of 6.2 g (0.022 mole) of 3,5-bis(1,1-dimethylethyl) -N,4-dihydroxybenzenecarboximidoyl chloride in absolute ethanol (60 ml). The mixture is stirred at room temperature for 18 hours, then evaporated to dryness (vacuum). The oil is dissolved in ethyl acetate (125 ml) and poured into water (125 ml). While stirring, the solution is acidified (pH 4.0-5.0) with 1N hydrochloric acid. The organic layer is separated, washed with water (2×100 ml), and dried (anhydrous magnesium sulfate). Evaporation of the organic layer leaves 5.0 g of crude material. Purification by flash chromatography (silica gel, ethyl acetate/hexane elution) gives 1.0 g (16%) of analytically pure 4-(5-amino-1,2,4-oxadiazol-3-yl)-2,6-bis(1,1-dimethylethyl)phenol, mp 202°-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155122 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-946d3625dfc84a0eabc4adea9c931b6f |
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| Source note | uspto-grants-1992_10 |
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