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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1022463Erstellt: 27. Oktober 2026

1,4-Benzodioxan → Methanone, (2-bromo-5-iodophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)-

https://huagongshe.com/reaction/1022463

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-BenzodioxanHCID 10301—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt2-Bromo-5-iodobenzoyl chlorideHCID 58340809—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethanone, (2-bromo-5-iodophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)-HCID 5834079888,5%

Reaktionsschritte

To a stirred solution of 2-bromo-5-iodo-benzoyl chloride (−158 g, 457 mmol) in DCM (1500 ml) was added benzo(1,4)-dioxane (65.8 ml, 549 mmol) at 0° C. To this reaction mixture, aluminum chloride (195.4 g, 1465 mmol) was added in portions. After stirring for overnight at room temperature, reaction mixture was poured into crushed ice. This was extracted with dichloromethane (1000 ml×2). Dichloromethane layer was washed with water (1000 ml), saturated aqueous sodium bicarbonate solution (1000 ml×2), brine (1000 ml), dried over sodium sulfate, and concentrated. The solid product was triturated with hexanes. The product was dried under vacuum to give 180 g of (2-bromo-5-iodo-phenyl)-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-methanone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722633B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-ef8c683df2d84731829d59d691fc2805
Quellennotizuspto-grants-2014_05