HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265161Generated: October 26, 2026
Ammonium Chloride → 2-Butyl-5-cyano-4-(1-hydroxy-1-methylethyl)-1-tritylimidazole
https://huagongshe.com/reaction/265161
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Acetyl-2-butyl-5-cyano-1-tritylimidazole | HCID 19036085 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Butyl-5-cyano-4-(1-hydroxy-1-methylethyl)-1-tritylimidazole | HCID 19036221 | — |
Reaction Steps
1 ml of a 2M solution of methylmagnesium iodide in tetrahydrofuran was added dropwise at room temperature, whilst stirring, to a solution of 840 mg of 4-acetyl-2-butyl-5-cyano-1-tritylimidazole [prepared as described in Preparation 5(ii)] in 15 ml of tetrahydrofuran, and the resulting mixture was stirred at 40° C. for 1 hour. The mixture was cooled, and then a saturated aqueous solution of ammonium chloride was added to it dropwise. The tetrahydrofuran layer was separated and concentrated by evaporation under reduced pressure. The concentrate was purified by column chromatography through silica gel, using a 2:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 539 mg of the title compound as a colorless solid, melting at 151°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646171 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-625976cf6e1d40f7a7d3beb93511db1b |
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| Source note | uspto-grants-1997_07 |
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