HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975212Generated: October 29, 2026
Water → 2,2,2-trifluoro-1-(3-methoxyphenyl)ethanone
https://huagongshe.com/reaction/975212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,2,2-trifluoro-1-(3-methoxyphenyl)ethanol | HCID 2829249 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2,2-trifluoro-1-(3-methoxyphenyl)ethanone | HCID 2759734 | — |
Reaction Steps
4.82 g (0.023 mol) of 2,2,2-trifluoro-1-(3-methoxyphenyl)ethanol and 0.4 g (0.0012 mol) of tetrabutylammonium hydrogen sulfate are dissolved in 100 ml of methylene chloride at room temperature. 14.4 ml (0.028 mol) of an approximately 12% strength sodium hypochlorite solution are metered in within 15 minutes with vigorous stirring and the mixture is stirred for a further 6 hours during which the reaction temperature rises to 26° C. The reaction mixture is added to 100 ml of water, the phases are separated, the aqueous phase is extracted several times with methylene chloride and the combined organic phases are washed with saturated aqueous sodium chloride solution. After drying the organic phase with sodium sulfate, the volatiles are distilled off. Following distillation of the crude product in a kugelrohr (0.2 mbar, 60°-70° C. bath temperature), 2.1 g (44% of theory) of 3-trifluoroacetylanisole are obtained. nD20 : 1.4773.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05608062 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-54638de163e34c6cb80914bf7378cad5 |
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| Source note | uspto-grants-1997_03 |
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