Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 15572247 | HCID 15572247 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15572312 | HCID 15572312 | — |
Reaction Steps
A mixture of 2.1 g. (6 mmoles) of 4,5-bis-(4-fluorophenyl)-2-(trifluoromethylthio)pyrrole and 1.3 g. (12 mmoles) of potassium tert-butoxide in 60 ml. of toluene was heated to reflux with stirring and then cooled to room temperature under nitrogen. A solution of 1.7 g. of benzoyl chloride in 15 ml. of toluene was then added and the reaction mixture stirred overnight at room temperature. The mixture was diluted with methylene chloride, which was washed with 10% aqueous sodium bicarbonate solution, dried and evaporated. The residue was purified by chromatography on Fisher 100-200 mesh silica gel (eluted by hexane and then by mixtures of hexane/toluene), followed by recrystallization from ethanol/water to afford 1.8 g. of colorless crystals, m.p. 105.5°-106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04267184 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-7002803bb6714e40943acd0a28e131ae |
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| Source note | uspto-grants-1981_05 |
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