Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 12227422 | HCID 12227422 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57323911 | HCID 57323911 | — |
Reaction Steps
To a suspension of 4.08 g of imidazole and 30 ml of dry methylene chloride, 1.78 g of thionyl chloride was added with ice-cooling. The resultant mixture was stirred for 30 minutes, followed by an addition of 2.10 g of 2-phenylthio-2'-hydroxyacetophenone. The thus-obtained mixture was stirred at room temperature for 2 hours. Ice water was then added to the reaction mixture, followed by its extraction with methylene chloride. The methylene chloride extract was then subjected to a post treatment in the same manner as in Example 10. The reaction product was separated by column chromatography, thereby obtaining 0.2 g of Isomer A (Compound 61) and 1.0 g of Isomer B (Compound 62) of 1-(2-hydroxyphenyl)-1-imidazolyl-2-phenylthioethylene as colorless crystals respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04740601 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-5351f6c57b014a2c88e6dc17e0619fbb |
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| Source note | uspto-grants-1988_04 |
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