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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2,4-Dichlorobenzoyl chlorideHCID 66645—
Edukt1-(4-Bromo-2-hydroxyphenyl)ethan-1-oneHCID 10727403—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,4-Dichloro-benzoic acid 2-acetyl-5-bromo-phenyl esterHCID 5978887584%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420066B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-4fed5d305a384154ad38efb590cc7f20
Quellennotizuspto-grants-2008_09