HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030091Generated: October 27, 2026
Sulfuric Acid → 2',4',5'-Trifluoroacetophenone
https://huagongshe.com/reaction/1030091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2,4,5-Trifluorobenzoyl chloride | HCID 145164 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2',4',5'-Trifluoroacetophenone | HCID 594417 | 47% |
Reaction Steps
194.5 g (1 mol) of 2,4,5-trifluorobenzoyl chloride were initially introduced into 100 ml of diethyl ether and heated to boiling under reflux. 1.1 mol of ethoxymagnesium malonic ester dissolved in 100 ml of ethanol and 125 ml of diethyl ether were then allowed to drop in in the course of 30 minutes and the mixture was stirred for 1 hour under reflux. After cooling, the reaction mixture was stirred into 500 ml of ice water and adjusted to a pH of 1 with concentrated sulphuric acid, and the organic material (345 g) was separated off. This organic material was dissolved in 300 ml of acetic acid and, after adding 37.5 ml of concentrated sulphuric acid, heated to reflux until evolution of CO2 had ended, which took 6 hours. The reaction mixture was then cooled and poured into water, and the organic phase was separated off and distilled. 83 g of product having a boiling point at 10 mbar of 63° to 64° C. were obtained. This corresponds to a yield of 47% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05104879 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-9a94c4ac70b74055bd9a1bf8cbf3ebcc |
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| Source note | uspto-grants-1992_04 |
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