HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094810Generated: November 2, 2026
Imidazole → Imidazole-1-carbothioic acid O-[1-(2-bromophenyl)-2,2,2-trifluoroethyl]-ester
https://huagongshe.com/reaction/1094810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 1-(2-Bromophenyl)-2,2,2-trifluoroethan-1-ol | HCID 57582369 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Imidazole-1-carbothioic acid O-[1-(2-bromophenyl)-2,2,2-trifluoroethyl]-ester | HCID 57582364 | 81.2% |
Reaction Steps
Thiophosgene (24.0 g, 210.0 mmol) was added portion-wise to a vigorously stirred suspension of imidazole (57.0 g, 840.0 mmol) in 1,2-dichloroethane (500 ml) under an atmosphere of nitrogen. After the addition, the reaction mixture was stirred at room temperature for 30 minutes. 1-(2-Bromophenyl)-2,2,2-trifluoro-ethanol (Preparation 55, 46 g, crude, about 140 mmol) in 1,2-dichloroethane (100 m) was added at room temperature. After the addition, the mixture was heated at reflux for 10 minutes. The reaction mixture was cooled then the solvent was evaporated in vacuo. The crude product was purified by column chromatography on silica gel eluting with petroleum ether, then petroleum ether:ethyl acetate (10:1) to afford the title compound as a yellow oil (41.5 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134007B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-e8217c93d9844f93aac1f085dfc68a59 |
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| Source note | uspto-grants-2012_03 |
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