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HRID 131148Erstellt: 26. Oktober 2026
Water → 2-Bromo-1-(2,4,6-trichlorophenyl)ethanone
https://huagongshe.com/reaction/131148
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 1,3,5-Trichlorobenzene | HCID 7950 | — |
| Edukt | Bromoacetyl bromide | HCID 61147 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Bromo-1-(2,4,6-trichlorophenyl)ethanone | HCID 21864946 | 69,3% |
Reaktionsschritte
A mixture of 1,3,5-trichlorobenzene (10.0 g, 55.1 mmol), 2-bromoacetyl bromide (5.0 mL, 57.8 mmol, 1.05 eq), and aluminum chloride (7.7 g, 57.8 mmol, 1.05 eq) was heated neat at 80° C. under argon for 17 h until a black precipitate is formed. The reaction was cooled to room temperature, and the resultant black mass was dissolved in ethyl acetate (500 mL). Water (200 mL) was added slowly at 0° C. to quench the reaction, and the biphasic layers were separated. The organic layer was then washed with water (2×150 mL) and brine (1×150 mL), dried (MgSO4), filtered, and evaporated in vacuo. Recrystallization from hexane gave 11.5 g (69.3%) of 2-bromo-1-(2,4,6-trichlorophenyl)ethanone as a fluffy white solid. 1H-NMR (DMSO-d6) δ 7.86 (s, 2H), 4.78 (s, 2H); Rf=0.28, 2% ethyl acetate-hexane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07384947B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-1f51f824f8ed43009701d9111938ea26 |
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| Quellennotiz | uspto-grants-2008_06 |
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