Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | HCID 59333358 | HCID 59333358 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 24700976 | HCID 24700976 | 92.3% |
Reaction Steps
To a solution of 1-(4-bromo-2-nitro-phenyl)-1H-imidazole (1.80 g; 6.72 mmol; 1 eq) in ethanol (90 mL) is added dehydrated tin chloride (7.58 g; 33.58 mmol; 5 eq). The reaction mixture is allowed to stir under reflux for 20 hours until completion of the reaction. The crude reaction mixture is then concentrated under vacuum. The resulting mixture is dissolved in water/ethyl acetate 1:2 (40 mL). The aqueous phase is basified until pH 9 is reached with solid hydrogen carbonate. The milky white aqueous phase is then extracted twice with ethyl acetate (2×100 mL). The combined organic phases are washed with brine (100 mL), dried over sodium sulfate and concentrated under vacuum to provide a beige powder. Purification by chromatography on silica gel (dichloromethane/methanol 97:3), afforded the title compound (1.47 g; 6.2 mmol; 92%) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513250B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-532aac8195f841d7af56d70b2bc28a96 |
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| Source note | uspto-grants-2013_08 |
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