Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| Reactant | Heptanenitrile, 7-bromo- | HCID 88737 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15067997 | HCID 15067997 | — |
Reaction Steps
A mixture containing 20.6 g (0.10 mole) of 3,5-di-t-butylphenol, 20.9 g (0.11 mole) of 7-bromoheptanenitrile, 4.0 g (0.10 mole) of sodium hydroxide and 250 ml of dimethylformamide was heated at 120° C. for about forty hours. The solvent was evaporated and the residue was added to 250 ml of water. The resulting oil was separated and dissolved in 250 ml of diethyl ether. The ether solution was washed twice with 250 ml portions of 10% sodium hydroxide, washed once with 250 ml water, dried over magnesium sulfate, and evaporated to give an oil which solidified on standing. The solid was recrystallized twice from methanol. The structure was confirmed by nuclear magnetic resonance spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04973731 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-e32e41fd8d154645b6d308e5c0bde38f |
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| Source note | uspto-grants-1990_11 |
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