Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptanol | HCID 8129 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178455735 | HCID 178455735 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178444041 | HCID 178444041 | 59.6% |
Reaction Steps
A solution of n-heptanol (3.5 g) in toluene (50 ml) was dropwise added to a suspension of sodium hydride (about 55%) (1.5 g) in toluene (50 ml). The mixture was agitated for 30 minutes, dropwise adding a solution of 3-(4-(2-(trans-4-ethylcyclohexyl)ethyl)phenyl)-6-chloropyridazine (5 g) obtained above, in toluene (100 ml), heating the mixture under reflux for 3 hours. The reaction solution was poured in water. The resulting organic layer was washed with water until the organic layer became neutral. After drying it over anhydrous magnesium sulfate, distilling off the solvent under reduced pressure and recrystallizing the residue from ethanol, the captioned 3-(4-(2-(trans-4-ethylcyclohexyl)ethyl)phenyl)-6-heptyloxypyridazine (3.7 g) was obtained. ##STR12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05213708 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-6b0db9bc305e4be180fb2f55055156f0 |
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| Source note | uspto-grants-1993_05 |
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