HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847543Generated: October 27, 2026
Hydrochloric Acid → 2-Chloro-1-(2,4,5-trifluorophenyl)ethan-1-one
https://huagongshe.com/reaction/847543
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 2',4',5'-Trifluoroacetophenone | HCID 594417 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-1-(2,4,5-trifluorophenyl)ethan-1-one | HCID 14793286 | — |
Reaction Steps
40.8 g (0.3 mole) of sulphuryl chloride were added dropwise at room temperature (22° C.) to 48 g (0.275 mole) of 2,4,5-trifluoroacetophenone (obtained according to Example 6), dissolved in 400 ml of dichloromethane, and the mixture was stirred until the end of the evolution of hydrogen chloride (about 2 hours). 600 ml of water were then added to the reaction mixture, the organic phase was separated off, and this was washed until neutral with sodium hydrogen carbonate solution and dried over magnesium sulphate, and the solvent was stripped off in a water pump vacuum. 48.6 g of 2,4,5- trifluoro-phenacyl chloride were obtained as an oily residue, which corresponds to 84.5 % of theory. The characterization of the product carried out as in Examples 9 to 15 gave a δ value of 5.29 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05142092 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-c3ddf329704e4930aa9100cbdeef4d2b |
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| Source note | uspto-grants-1992_08 |
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