HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030092Generated: October 27, 2026
Hydrochloric Acid → 2-Chloro-1-(2,4,5-trifluorophenyl)ethan-1-one
https://huagongshe.com/reaction/1030092
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 mol) of sulphuryl chloride were added dropwise at room temperature (22° C.) to 48 g (0.275 mol) of 2,4,5-trifluoroacetophenone (obtained according to Example 110)dissolved in 400 ml of dichloromethane and the mixture was stirred until evolution of hydrogen chloride had ended (about 2 hours). The reaction mixture was then added to 600 ml of water, the organic phase was separated off, 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-trifluorophenacyl chloride were obtained as an oily residue, which corresponds to 84.5% of theory. The characterization of the product carried out as in Examples 113 to 119 yielded a & value of 5.29 ppm.
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-dd952ed04b3c4e079bf42ebf80f3cb8d |
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| Source note | uspto-grants-1992_04 |
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