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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2075841Erstellt: 26. Oktober 2026

Benzeneacetyl chloride, 4-bromo- → HCID 57441117, Verbindung

https://huagongshe.com/reaction/2075841

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneacetyl chloride, 4-bromo-HCID 181552—
Edukt2-(Trimethylsilyl)benzofuranHCID 13148489—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 57441117HCID 5744111717,4%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Benzofuran-2-yl-trimethyl-silane (3.4 g, 17.86 mmol) was dissolved in methylene chloride (40 mL) and cool to −78° C. 4-Bromophenyl-acetyl chloride (19.65 mmol, 1.1 equiv.) was added at this temperature. Under vigorous stirring, a solution of TiCl4 (23 mL, 1M, 23.2 mmol, 1.3 equiv.) in CH2Cl2 was added dropwise and stirring continued for 20 min. Then the reaction was quenched with H2O (100 mL), cooling bath was removed and the mixture was allowed to warm up to room temperature. It was then diluted with H2O (100 mL) and extracted with CH2Cl2 (3×). Organic layers were combined, washed with brine, dried over MgSO4, solvent evaporated. Crude product thus obtained was subject to column purification. (silica gel, 10% EtOAC/Hexane). 980 mg of 1-Benzofuran-2-yl-2-(4-bromo-phenyl)-ethanone was obtained in 17% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07923446B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-4f05a23f98e74ec0b28a50c12ce96360
Quellennotizuspto-grants-2011_04