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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantThiophosgeneHCID 10040—
Reactant1-(2-Bromophenyl)-2,2,2-trifluoroethan-1-olHCID 57582369—
Solvent1,2-DichloroethaneHCID 11—
ProductImidazole-1-carbothioic acid O-[1-(2-bromophenyl)-2,2,2-trifluoroethyl]-esterHCID 5758236481.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134007B2
Source datasetuspto-grants-2012_03
ORD IDord-e8217c93d9844f93aac1f085dfc68a59
Source noteuspto-grants-2012_03