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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 900367Erstellt: 24. Oktober 2026

4-Bromobenzoyl chloride → (4-Bromo-phenyl)-(2-butyl-benzofuran-3-yl)-methanone

https://huagongshe.com/de/reaction/900367

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromobenzoyl chlorideHCID 68515—
Edukt2-ButylbenzofuranHCID 77951—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelDichloromethaneHCID 6344—
Produkt(4-Bromo-phenyl)-(2-butyl-benzofuran-3-yl)-methanoneHCID 5965597436%

Reaktionsschritte

A solution of 2-n-butylbenzofurane (19.8 g, 114 mmol) and 4-bromobenzoyl chloride (25.0 g, 114 mmol) in dry dichloromethane (300 mL, 0.4 M) was cooled to 0° C. and treated with AlCl3 (16.6 g, 1.1 equiv., 125.4 mmol) in 3 portions. After the additions were complete, the solution was stirred for 3 h and carefully added to ice water. After separation, the aqueous layer was extracted with dichloromethane (2×200 mL) and the combined organic layers were washed with water, sat'd aq NaCl, dried over anhydrous MgSO4, filtered and concentrated in vacuo. Purification by flash column chromatography (1-2% ethyl acetate in heptane) afforded (4-bromo-phenyl)-(2-butyl-benzofuran-3-yl)-methanone (14.6 g, 36%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07358248B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-7b7e41567f2b4f37b192ea9201092184
Quellennotizuspto-grants-2008_04