Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178431338 | HCID 178431338 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178431335 | HCID 178431335 | 74.6% |
Reaction Steps
94.13 g (0.317 mole) of alpha-(2,2-dimethyl-4H-1,3-benzodioxin-8-yl)-1H-imidazole-4-methanol hydrochloride (prepared in Example 3.1. or 3.5.) are introduced into 1 liter of anhydrous liquid ammonia. The solubilization of the reagent is completed by the addition of 1 liter of tetrahydrofuran. 14.6 g (0.634 mole) of sodium are then added piece by piece. 5 minutes after the sodium has disappeared, 34 g of ammonium chloride are added and the reaction mixture is stirred for 30 minutes. There is then added 1.56 liter of a 10% solution of methanol in toluene. The ammonia is then evaporated on a water-bath. 780 ml of water are then added and the organic phase is separated. The aqueous phase is extracted twice with 500 ml of toluene. The organic phases are combined and washed with 1 liter of water, then dried over anhydrous sodium sulfate and distilled under reduced pressure. The residue obtained is recrystallized from 900 ml of boiling acetone. There are thus obtained 57.8 g of 4-[(2,2-dimethyl-4H-1,3-benzodioxin-8-yl)methyl]-1H-imidazole; M.P.: 160°-170° C. Yield: 74.6% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04814343 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-31c00bc2485c4e72a073336af5f67a44 |
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| Source note | uspto-grants-1989_03 |
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