HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29251Erstellt: 26. Oktober 2026
Triethylamine → 2,4-Dichloro-benzoic acid 2-acetyl-5-bromo-phenyl ester
https://huagongshe.com/reaction/29251
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,4-Dichlorobenzoyl chloride | HCID 66645 | — |
| Edukt | 1-(4-Bromo-2-hydroxyphenyl)ethan-1-one | HCID 10727403 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,4-Dichloro-benzoic acid 2-acetyl-5-bromo-phenyl ester | HCID 59788875 | 84% |
Reaktionsschritte
Triethylamine (14.6 mL, 104.6 mmol) was added to a solution of 1-(4-Bromo-2-hydroxy-phenyl)-ethanone (15.0 g, 96.8 mmol) dissolved in dichloromethane (200 mL). The resulting solution was cooled to 0° C. at which time 2,4-dichloro-benzoyl chloride, dissolved in 50 mL dichloromethane was added dropwise over 30 minutes. The resulting mixture was allowed to warm to ambient temperature and stir at this temperature for an additional 16 hours. After this time, the reaction mixture was concentrated via rotary evaporation and then dissolved in EtOAc and washed twice with water and once with a saturated NaHCO3 solution. The organic portion was dried (MgSO4), filtered and concentrated to give the desired product (22.7 g, 84%) which was used without further purification. 1H-NMR (DMSO) δ 8.18 (d, 1H), 7.96 (d, 1H), 7.82 (s, 1H), 7.64 (m, 3H), 2.53 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07420066B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-4fed5d305a384154ad38efb590cc7f20 |
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| Quellennotiz | uspto-grants-2008_09 |
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