HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353009Generated: October 30, 2026
2-Thiocresol → 2-(4-Chlorophenyl)-4-[[(2-methylphenyl)thio]methyl]-1-[4-(methylsulfonyl)phenyl]-1h-imidazole
https://huagongshe.com/reaction/1353009
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Thiocresol | HCID 8712 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-chloromethyl-2-(4-chlorophenyl)-1-(4-(methylsulfonyl)phenyl]-1H-imidazole | HCID 10809843 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Chlorophenyl)-4-[[(2-methylphenyl)thio]methyl]-1-[4-(methylsulfonyl)phenyl]-1h-imidazole | HCID 22997912 | — |
Reaction Steps
To a solution of 4-chloromethyl-2-(4-chlorophenyl)-1-(4-(methylsulfonyl)phenyl]-1H-imidazole (Example 159, Step 1) (250 mg, 0.656 mmol) and o-thiocresol (163 mg, 1.31 mmol) in 5 ml of dry dimethylformamide was added anhydrous potassium carbonate (226 mg, 1.64 mmol). The mixture was stirred rapidly overnight at room temperature. The mixture was then partitioned between ethyl acetate and water. The aqueous layer was further extracted with ethyl acetate, the combined organic extracts washed with brine, and dried over sodium sulfate. The solution was filtered and concentrated. Chromatography of the residue over silica gel using 40% ethyl acetate in hexane gave the title compound as a very pale yellow solid (210 mg): mp (DSC) 51° C. Anal. Calc'd. for C24H21ClN2O2S2 (MW 469.03): C, 61.46; H, 4.51; N, 5.97. Found: C, 61.16; H, 4.50; N, 5.86.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220770B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-2d5e508ca6964b12a2886da9e182e2c7 |
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| Source note | uspto-grants-2007_05 |
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